- Original Article
- Serum Vitamin A Leveland Immunization Status in Serologically Confirmed Measles Patients
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Kyung Hwa Park, Seung Hee Choe, Chang Hwi Kim, Dong Hwan Lee, Sang Mann Shin, Sang Jhoo Lee
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Clin Exp Pediatr. 1996;39(2):187-194. Published online February 15, 1996
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Purpose : To know the relationship between serum vitamin A level and clinical symptoms in measles patients and to re-evaluate the measles vaccination schedule, we performed this study.
Methods : From Jan. to Jun. 1994, we checked serum vitamin A levels and compared with
clinical symptoms, laboratory findings, complications and vaccination status in 153 patients with positive measles IgM by ELISA.
Results :... |
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- The Influence of the Use of Iodine during Perinatal Period on the Screening Test for Congenital Hypothyroidism
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Gyu Bum Cho, Dong Hwan Lee, Sang Jhoo Lee
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Clin Exp Pediatr. 1996;39(2):195-206. Published online February 15, 1996
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Purpose : This study was performed to detect the diseases of congenital hypothyroidism by the neonatal mass screening test early and to demonstrate the possible role of topical iodinated antiseptics(povidone-iodine, PVP-Ⅰ) on transient hyperthyrotropinemia in newborn infants.
Methods : We performed neonatal screening tests for inborn errors of metabolism since 1985 by Guthrie test for PKU, maple syrup urine disease, histidinemia,... |
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- Immunologic Considerations in the Pathogenesis of Chronic and Recurrent Sinusitis in Children
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Jun Ki Jung, Bok Yang Pyun, Sang Mann Shin, Sang Jhoo Lee
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Clin Exp Pediatr. 1996;39(2):207-217. Published online February 15, 1996
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Purpose : Although the chronic sinusitis is one of the most common and troublesome respiratory diseases in children, the pathogenesis still remains unclear. It is suggested that many of the immunologic factors including allergic conditions may contribute the nasal inflammatory changes. This study was designed to evaluate and demonstrate the possible role of various immunologic factors on the pathogenesis of... |
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- Case Report
- A Case of Castleman's Disease in Childhood
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Jong Yoo Lee, Kyung Bae Park, Joon Soo Park, Sang Chul Park, Sang Man Shin, Sang Jhoo Lee, Young Moo Kyu, Ui Han Kim
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Clin Exp Pediatr. 1996;39(2):291-295. Published online February 15, 1996
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Castleman's disease(CD) is rare in childhood. It is defined as a localized nodal hyperplasia in mediastinum or cervical area. It is also called angiofollicular lymph node hyperplasia, lymph nodal hamartoma, giant lymph node hyperplasia. It was first described in 1956 by Castleman et al. as a lesion of mediastinal mass. The etiology of CD is not clear. The histologic classification... |
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- Original Article
- Intracraial Hemorrhage in Premature and Low Birth Weight Infants by Craniosonography
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Seung Hee Choi, Jae Ock Park, Sang Man Shin, Sang Jhoo Lee
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Clin Exp Pediatr. 1995;38(6):752-759. Published online June 15, 1995
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Purpose : Intrabventricular hemorrhage is a common neuropathologic finding in premature and low birth weight infants. It is deeply related with neonatal death and neurologic sequelae. We want to know the incidence and the relating factors of intracranial hemorrhage in premature and low birth weight infants.
Methods : We performed craniosonography in 170 premature and low birth weight infants in 3-7... |
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- Case Report
- A Case of Congenital Lipoid Adrenal Hyperplasia
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Hae Kyung Lee, Dong Hwan Lee, Sang Jhoo Lee
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Clin Exp Pediatr. 1995;38(4):567-573. Published online April 15, 1995
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Congenital lipoid adrenal hyperplasia is the rarest type among salt losing types of congenital adrenal hyperplasia. The defect of this disorder is in the cholesterol side chain cleavage enzyme(P450SCC)which converts cholesterol to pregnenolone.
We experienced a case of 20,22 desmolse deficiency in a 21-day old phenotypically female who was admitted to our hospital due to lethargy and dark skin pigmentation. The... |
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- A Case of Sjören-Larsson Syndrome
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Kil Joon Lee, Jong Bock Kim, Dong Hwan Lee, Sang Man Shin, Sang Jhoo Lee
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Clin Exp Pediatr. 1994;37(12):1757-1761. Published online December 15, 1994
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Sjören-Larsson Syndrome is a rare disorder chracterized by congenital icthyosis, spastic diplegia or tetraplegia and mental retardation. The inheritance is autosomal recessive, due to deficiency of alcohol dehydrogenase activity of fatty acid matabolism.
We have experienced a case of Sjören-Larsson Syndrome in a 16 month-old male children who have dried thick skin, developmental delay, and spastic diplegia.
He was much improved clinically... |
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- Original Article
- Ultrasonographic Measurement of the Neonatal Adrenal Glands
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Hae Kyung Lee, Jae Ock Park, Chang Hwi Kim, Sang Man Shin, Sang Jhoo Lee
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Clin Exp Pediatr. 1993;36(8):1101-1106. Published online August 15, 1993
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To determine the normal neonatal adrenal gland size, ultrasonographic examinations were performed in 145 newborn infants. They were divided into 3 groups according to the days of age. The group I is 1~3 days, group II is 6~9days and group III is 21~50days of age.
1) The adrenal gland size was as follows.
In group I, the length was 29.05mm and the... |
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- Case Report
- A Case of Laryngeal Cleft
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Yong Sik Min, Hye Kyu, Jun Soo Park, Dong Hwan Lee, Sang Jhoo Lee, Hyun Sook Hong
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Clin Exp Pediatr. 1993;36(7):1016-1024. Published online July 15, 1993
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Laryngotracheoesophageal cleft is a rare congenital anomaly characterized by a midline defect of variable length between the posterior larynx and trachea and the anterior wall of the esophagus which was first reported by Richter in 1792.
The male, birth weight 2780 gm, was born our hospital. After birth the infant breathed spontaneously, cried immediately but weak and did well initially but... |
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- A Case of Syndrome Associated with Colonic Atresia
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Si Whan Koh, Joon Soo Park, Kyung Hwan Oh, Dong Hwan Lee, Sang Jhoo Lee, Chul Moon
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Clin Exp Pediatr. 1993;36(7):1030-1033. Published online July 15, 1993
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The association of colonic atresia in patients with Down syndrome is a rare anomaly. The incidence of congenital atresia of the gastrointestinal tract has been estimated to be about one in 1500 births. Colonic atresia is rarer still, and is throut to comprise about 5% to 10% of this group. This intestinal atresia occurs in about 30% to 50% of... |
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- Original Article
- The Change of Anti-HBs Titer after Hepatitis B Vaccination in Newborn According to Dosage and Time
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Joon Young Lee, Yong Sik MIn, Chang hwi Kim, Sang Jhoo Lee
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Clin Exp Pediatr. 1993;36(5):656-663. Published online May 15, 1993
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We studied anti-HBs titer, positive and effective rate in relation to dosages(5, 10) and time interval after third vaccination in 23 infants born to HBsAg negative mother. The babies were divided into two groups. In one group(n=12), 5 of Hepavax was administered intramusculary at 1 month, 2 months and 6 months age, in other group (n=11), 10 of Hepavax at... |
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- Pterin & DHPR Measurement and DNA Analysis in Korean PKU Patients
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Chol Hee Chong, Hye Yong Lee, Dong Hwan Lee, Sang Jhoo Lee, Ki Weon Cha, Jeong Bin Yim, Yoshiyuki Okano
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Clin Exp Pediatr. 1993;36(12):1681-1690. Published online December 15, 1993
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Phenylketonuria in metabolic disorder that results from a deficiency of the hepatic phenylalanine hydroxylase. But among patients with hyperphenylalaninemia, the defect resides in one of the enzymes necessary for production or recycling of tetrahydrobiopterin (BH4). The reduction of BH4 affects not only phenylalanine metabolism but also formation of the tyrosine related neurotransmitter, dopamin and tryptophan related neurotransmitter, serotonin.
Administration of L-dopa... |
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- A Study of Screening for Anemia in 9 Month Old Infants in Well Baby Clinic
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Yong Sik Min, Jae Ock Park, Sang Man Shin, Sang Jhoo Lee
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Clin Exp Pediatr. 1993;36(11):1516-1525. Published online November 15, 1993
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Iron deficiency remains the most common cause of anemia in infants and children despite increasing availability of iron-fortified foods. We screened out anemia in 9-month old infants in well baby clinic to know the prevalence of anemia and the weaning status.
The results were as follows.
1) Among 345 infants screened, 24 infants(7%) were found to have anemia.
2) The king of anemia... |
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- Intractranial Hemorrhage in Full-Term Neonates by Ultrasonography
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Chang Gyu Lim, Joon Soo Park, Woo Ryong Lee, Jae Ock Park, Sang Mann Shin, Sang Jhoo Lee
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Clin Exp Pediatr. 1993;36(11):1570-1577. Published online November 15, 1993
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Intracranial hemorrhage is the most common neuropathologic finding in premature infants. But in full-term infants, It is less common and rarely causes death. We found out intracranial hemorrhages in 21 full-term neonates by real-time neurosonography and concluded as followings.
1) Among 21 neonates, 17 infants were male and 4 infants were female.
2) In 11(52.3%) infants the hemorrhage was detected within 7... |
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- A Clinical Study of Histiocytosis Syndrome
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Hye Yong Lee, Chul Hee Chung, Won Suk Suh, Sang Mann Shin, Sang Jhoo Lee
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Clin Exp Pediatr. 1993;36(10):1417-1425. Published online October 15, 1993
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We made a clinical study on 10 cases of histiocytosis syndrome who had been admitted to the pediatric department of Soon Chun Hyang University Hospital from Jan 1982 to Dec. 1991.
The results were obtained as follows
1) The sex incidence revealed male predominance with the ratio 4:1.
2) Among 10 cases, 4 cases were classified as eosinophilic granuloma, 1 case as Letterer-Siwe... |
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- Case Report
- A Case of Prune Belly Syndrome ssociated with Turner Syndrome
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Chang Soo Oh, Sang Muk Choi, Jae Ock Park, Chang Hwi Kim, Sang Jhoo Lee
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Clin Exp Pediatr. 1992;35(7):978-983. Published online July 15, 1992
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The Prune belly syndrome is a rare congenital anomaly characterized by lax, wrinkled abdominal wall, cryptorchidism and urinary tract anomalies. But it has a wide spectrum of clinical presentation and combine with other anomalies such as pulmonary, skeletal, digestive, cardiovascular and other system. We experienced a case of prune-belly syndrome associated with Turner syndrome in a 18 month old female... |
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- A Case of Neonatal Hypothyroidism due to Maternal TSH-Binding Inhibitor Immunoglobulin
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Myung Lye Kim, Rhie Choi, Dong Hwan Lee, Sang Jhoo Lee
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Clin Exp Pediatr. 1992;35(6):804-808. Published online June 15, 1992
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Neonatal screening for congenital hypothroidism is important because of the possibility that mental retardation may be avoided if treatment started early.
A 1 day old patient was admitted to our department of Pediatrics for congenital hypothyroidism screening. The mother was 33 years old and had been on thyroid replacement therapy since 32 years of age. During the pregnancy she was euthyroid... |
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- A Nonfamilial Case of Multiple Juvenile Polyposis
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Jin Seop Shim, Sang Mook Choi, Eun Mi Kim, Jae Ock Park, Sang Jhoo Lee, Chan Sup Shim, Chul Moon
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Clin Exp Pediatr. 1992;35(6):851-861. Published online June 15, 1992
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Juvenile polyps are common and cause painless hematochezia in preschool and school-aged children. Juvenile polyps of the colon are usually solitary and considered to be inflammatory of hamatomatous in nature without malignant potential.
Multiple juvenile polyposis is characterized by large numbers withch is spread to the colon or throughout the gastrointestinal tract.
We experienced a nonfamilial multiple juvenile polyposis in a... |
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- Original Article
- A Study of Serologically Confirmed Measles
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Sang Mook Choi, Chang Soo Oh, Sang Chul Park, Chang Hwi Kim, Sang Jhoo Lee
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Clin Exp Pediatr. 1992;35(4):508-514. Published online April 15, 1992
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Forty one cases of serologically confirmed measles(positive measles specific IgM antibody) were evaluated among 55 cases of clinically diagnosed measles admitted to Soon Chun Hyang University Hospital from May to August 1990.
The results were as follows:
1) Sex ratio was 1.6 : 1 with male predominance in 41 cases, 13 cases(31.7%) were vaccinated and 28 cases(68.3%) were unvaccinated. Primary vaccine failure... |
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- Case Report
- A Case of Neonatal Hydrometrocolpos Causing Urinary Obstruction
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Chang Soo Oh, Myung Lye Kim, Byung Tae Kim, Sang Jhoo Lee, Soo Hyoung Seo
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Clin Exp Pediatr. 1992;35(11):1597-1601. Published online November 15, 1992
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Neonatal hydrometrocolopos is a rare congenital anomaly, which is thought to be caused by both vaginal obstruction such as imperforate hymen, transverse vaginal septum or vaginal atresia and sufficient maternal estrogenic stimulation to provoke secretion from the glands in the neonatal reproductive tract. The presence of lower abdominal mass in a female infant should always arouse the suspicion of hydrometrocolpos... |
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- Original Article
- A Clinical Study in Phenylketonuria
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Hye Kyeong Nam, Jin Seop Shim, Dong Hwan Lee, Sang Jhoo Lee, Ki Weon Cha, Jeong Bin Yim
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Clin Exp Pediatr. 1992;35(1):69-79. Published online January 15, 1992
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Thirteen cases of phenylketonuria who were diagnosed at department of pediatrics, Soonchunhyang University Hospital, and four cases at other hospitals and other countries from July, 1984 to April, 1991 were reviewed and analyzed.
The results were as follow: 1) All 17 cases were between the age of 3 days and 19 years, and the male to female ratio was 1.43:1. 2)... |
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- Case Report
- Cases of Omental Cyst
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Ju Seok Maeng, Hae Kyung Lee, Jae Ock Park, Sang Jhoo Lee, Chul Moon, Dong Wha Lee
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Clin Exp Pediatr. 1992;35(1):129-134. Published online January 15, 1992
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A 3-year-old female patient was admitted due to marked abdomainal distension. Her mother has been noticed the abdominal distension since birth, and the abdomen was enlarged progressively, but there were no subjective symptoms such as abdominal pain, vomiting nor indigestion. The radiographic findings showed huge intraabdomainal mass anterior to intestine which had septated fluid collection in it. Omental cyst was... |
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- Original Article
- Two cases of cyclopia in twin.
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Joon Soo Park, Si Hwan Kho, Dong Hwan Lee, Sang Jhoo Lee, So Young Jin
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Clin Exp Pediatr. 1991;34(5):700-706. Published online May 31, 1991
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A Cyclopia in which the elements of the two eyes are completely or partially fused to form an
apparently single eye in the middle of the forehead, is part of an anomaly involving not only the eyes
themselves but also the anterior part of the brain and the mesodermal structures in the midline.
We have experienced two cases of Cyclopia in twin.
The autopsy... |
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- A case of Mosaic trisomy 8.
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Hye Kyung Nam, Dong A Lee, Dong Hwan Lee, Sang Jhoo Lee
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Clin Exp Pediatr. 1991;34(4):553-557. Published online April 30, 1991
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Cardinal clinical features of trisomy 8 are as follow: Absent patellae; mental retardation; facies
notable or its anteverted nose, long philtrum, micrognathia and malformed ears; flexion deformities
of the fingers or toes, deep plantar V-shaped cleft between the first and third interdigital web of foot,
“pH capitonne”. More than 35 patients have been identified as having trisomy 8.
The authors experienced a patient of... |
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- Clinical review of abdominal masses in infants and children.
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Dong A Lee, Woo Ryoung Lee, Jae Ock Park, Chang Hwi Kim, Sang Jhoo Lee
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Clin Exp Pediatr. 1991;34(3):380-387. Published online March 31, 1991
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We reviewed 34 patients with palpable abdominal mass among 5,920 infants and children who
admitted to the department of pediatrics of Soon Chun Hyang University from Jun. 1, 1986 to Aug.
31，1989.
The results were as follows:
1) The incidence was 0.57% and the male: female ratio was 1:1.3. The mass was noted before 1
year of age in 23.5% of cases and under 5 years... |
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- Two cases of islet cell hyperplasia with nesidioblastosis.
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Myeong Ku Cho, Kyeong Bae Park, Gyu Bum Cho, Dong Hwan Lee, Sang Jhoo Lee, D.H Lee
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Clin Exp Pediatr. 1991;34(2):273-280. Published online February 28, 1991
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Hypoglycemia due to Hyperinsulinism is associated with nesidioblastosis, islet cell hyperplasia or
adenoma.
We experienced two newborn infants suffering from recurrent attacks of hypoglycemia, they were
underwent a subtotal pancreatectomy for suspected islet cell dysmaturation syndrome. No tumor was
found, but histology revealed islet cell hyperplasia and nesidioblastosis.
After surgery one case who was treated with diazoxide, had persistent hypoglycemia but the other
showed normal glucose... |
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- Two cases of meconium peritonitis.
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Hye Kyung Nam, Dong Hwan Lee, Sang Jhoo Lee
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Clin Exp Pediatr. 1991;34(2):256-260. Published online February 28, 1991
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Meconium peritonitis is a non-bacterial foreign body and chemical peritonitis occurring during
intrauterine or early neonatal life as the result of an abnormal communicatiion between the bowel
contents and the peritonesal cavity.
We experienced two cases of meconium peritonitis, diagnosed in according to the clinical and
radiologic features, in two female neonates who had the chief complaint of vomiting and abdominal
distention. A brief review... |
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- Body part identification in 1-to 5-year-old children.
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Rhie Choi, Ju Seok Maeng, Dong Hwan Lee, Sang Jhoo Lee
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Clin Exp Pediatr. 1991;34(12):1647-1654. Published online December 31, 1991
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Until recently, minimal information on the development of body part identification in young
children has been available although several developmental assessments include items that involve
pointing to or naming body part.
The purpose of this study was to examine the sequence in which body parts are learned and can be
identified by very young children.
The 360 children who 1-to 5-year-old were tested during the... |
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- Clinical and statistical observation for very low birth weight infants.
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Sung Shin Park, Ji Hee Jung, Dong Hwan Lee, Sang Jhoo Lee
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Clin Exp Pediatr. 1991;34(12):1629-1640. Published online December 31, 1991
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We made clinical and statistical observation of 90 very low birth weight infants who were admitted
at Soonchunhyang university hospital during the 6 years period from January 1985 through December
1990.
The result obtained were as follows:
1) The incidence of very low birth weight infant during 6 years period was 0.68%, and the
mortality rate was 488/1000 very low birth weight infants.
2) There was no obvious... |
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- Two cases of thymolipoma.
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Rhie Choi, Young Chang Kim, Hak Joo Cha, Sang Jhoo Lee, cheol Sae Lee, Jung Ki Ro, Seung Ha Yang, Chang Jin Kim
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Clin Exp Pediatr. 1991;34(11):1605-1611. Published online November 30, 1991
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Thymolipoma is a benign anterior mediastinal tumor composed of thymic tissue and mature adipose
elements. The tumor is so rare that only 60 cases are reported in the world, and only 2 cases are reported in
Korea.
We have experienced two cases of thymolipoma in two thirteen-year-old boys. One had had chest pain and
exertional dyspnea for 1 month but the other had no... |
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- A case of 11q deletion syndrome.
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Hye Kyeong Nam, Rhee Choi, Chang Hwi Kim, Sang Jhoo Lee
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Clin Exp Pediatr. 1991;34(11):1587-1592. Published online November 30, 1991
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11q-syndrome is a rare chromosomal anomaly.
We experienced a case of llq deletion syndrome in a female infant. It was diagnosed by clinical
features and chromosomal study. She had multiple anomalies such as flat occiput, hypertelorism, low
set malformed ear, anteverted nostril, small carp-shaped mouth, micrognathia, hypertrophic pyloric
stenosis and ventricular septal defect.
Chromosomal study showed partial terminal deletion of the long arm of chromosome... |
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- Adrenocortical carcinoma in a twelve month old male infant.
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Woo Ryoung Lee, Kyoung Whan Oh, Chang Hwi Kim, Sang Jhoo Lee
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Clin Exp Pediatr. 1991;34(1):137-143. Published online January 31, 1991
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Adrenocortical carcinoma is a rare disease in childhood. Most of these carcinomas are functional, produc-
ing endocrine abnormalities such as Cushing syndrome, virilization, precocious puberty, hyperaldosteronism
or feminization.
We experienced a case of adrenocortical carcinoma in a 12 month old male infant who exhibited features
of Cushing syndrome, Virilization, precocious puberty and hyperaldosteronism, which were due to functional
adrenocortical carcinoma. Microscopic examination revealed cellular pleomorphism... |
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- A case of congenital lactic acidosis.
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Suk Min Choi, Myeong Ku Cho, Dong Hwan Lee, Sang Jhoo Lee, Kikumaro Aoki, Shuichi Yamaguchi
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Clin Exp Pediatr. 1991;34(1):95-100. Published online January 31, 1991
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The congenital lactic acidosis represent a sizable group of metabolic disorders.
They are in all likelihood genetically determined, and they are clearly heterogenous. They may be
considered broadly as disorders of pyruvate metabolism in which there are two general categories:
defects in gluconeogenesis and defects in pyruvate oxidation.
We experienced a case of congenital lactic acidosis in neonate who was diagnosed by urinary
organic acid... |
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- Cystinurua in Siblings.
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Sung Ik Cho, Min Yong Oum, Jae Ock Park, Dong Hwan Lee, Sang Jhoo Lee
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Clin Exp Pediatr. 1990;33(3):351-359. Published online March 31, 1990
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We report cystinuria in siblings. Renal colic, hematuria, dysuria and stone passage were developed
in younger brother (4 year 6 month old boy). But the elder sister (6 year old girl) had no specific
symptoms nor signs.
The identification of the disease was proved by cyanide nitroprusside test and amino acid analysis
of urine.
In our patients the chromatographic amino acid patterns of urine showed... |
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- A Case of Sirenomelia.
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Hyun Kuk Kim, Sung Ik Cho, Byoung Tae Kim, Hak Jhoo Cha, Sang Jhoo Lee
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Clin Exp Pediatr. 1990;33(2):241-245. Published online February 28, 1990
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A neonate weighing 960 gm with undetermined sex was born after 32 weeks of gestation. The baby
had multiple abnormalities such as fused lower extremities, abcence of the anus and external
genitalia, meningomyelocele, right anortia, anomalous ribs, pulmonary hypoplasia, renal agenesis and
rectal agenesis.
The diagnosis was established by physical and autopsy findings.
A brief review of literature was made. |
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- Glucose-6 Phosphate Dehydrogenase Deficiency.
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Meen Jai Lee, Sang Eun Lee, Dong Whan Lee, Sang Jhoo Lee, Sang Chul Park
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Clin Exp Pediatr. 1990;33(2):212-219. Published online February 28, 1990
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Glucose-6-phosphate dehydrogenase(G-6PD) deficiency is the most common disease-producing
enzyme deficiency of human beings, but extremely rare in Korea. Four well-characterized clinical
syndromes are recognized: acute, oxidative stress(drug or infection) induced hemolytic anemia;
neonatal hyperbilirubinemia; favism and chronic nonspherocytic hemolytic anemia. We have experi-
enced a case of G-6PD deficiency in child associated with chronic hemolytic anemia and exacerba-
tions of hemolysis by infection and drug... |
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- A Case of Nonimmunologic Hydrops Fetalis Associated with Down Syndrome.
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Sang Eun Lee, Meen Jai Lee, Dong Hwan Lee, Sang Jhoo Lee
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Clin Exp Pediatr. 1990;33(2):205-211. Published online February 28, 1990
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We experienced a case of nonimmunologic hydrops fetalis associated with Down syndrome.
The patient had generalized edema with severe scrotal swelling and abdominal distension.
A roentgenogram showed bilateral pleural effusion and ascites. The chromosomal study revealed
21 trisomy.
On autopsy, there were pleural fluid and ascites as well as pericardial fluid. Small ASD and
incomplete lobation of the right lung were detected.
Chromosomal abnormalities should always... |
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- A Clinical and Diagnostic Study of the Allergic Rhinitis in Children.
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Hyun Kuk Kim, Min Yong Oum, Bok Yang Pyun, Sang Jhoo Lee
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Clin Exp Pediatr. 1990;33(2):189-195. Published online February 28, 1990
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Recently many studies and development of allergology especially in allergic rhinitis have been
carried out and the number of allergic rhinitis patients has been increased.
In order to get basic clinical information, the authors performed clinical and diagnostic analysis
with 132 cases complaining of nasal stuffness, watery rhinorrhea or sneezing who visited the out-
patient department of Pediatrics, Soon Chun Hyang University Hospital from... |
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- Clinical Evaluation in Lipoid Pneumonia.
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Myeong Ku Cho, Suk Min Choi, Dong Hwan Lee, Sang Jhoo Lee
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Clin Exp Pediatr. 1990;33(12):1656-1661. Published online December 31, 1990
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Seven cases of lipoid pneumonia in infant who were admitted to department of pediatrics, Soon
Chun Hyang University Hospital from July 1988 to March 1990 were reviewed and analysed.
The results were as follows:
1) All cases were taken shark liver oil (squalene®) forcefully in supine position
2) Out of 7, all cases were between the age of 3 months and 6 months, and the male... |
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- A Study on Lighting in school.
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Kyung Hwan Oh, Woo Ryung Lee, Sang Cheol Park, Dong Hwan Lee, Sang Jhoo Lee
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Clin Exp Pediatr. 1990;33(12):1623-1630. Published online December 31, 1990
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The students had to spend their most of times in school. It was supposed that the lighting of
classrooms greatly affected the growth and development and visual acuity of students.
The illuminance was measured in 12 classrooms of Chun An city (primary, middle and high school)
from July to September, 1989.
To evaluate the present status and problems of lighting in classrooms, we analyzed... |
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- A Case of Cloacal Exstrophy.
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Kyung Hwan Oh, Joon Soo Park, Hak Joo Cha, Sang Jhoo Lee
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Clin Exp Pediatr. 1990;33(11):1574-1578. Published online November 30, 1990
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Cloacal exstrophy is a rare congenital anomaly. This anomaly results from failure of cloacal
cpntatinn with the persistence of ? into which ilpiiir* and a rndirnAntary
hind gut open. We have experienced in a 1-day old male neonate a typical case of cloacal exstrophy
associated with omphalocele, genital anomaly, imperforated anus, meningocele, spina bifida, widely
separated symphysis and equinovarus.
A brief review of related literatures was made. |
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- A Case of Crohn's Disease.
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Suk Min Choi, Myeong Ku Cho, Sang Man Shin, Sang Jhoo Lee
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Clin Exp Pediatr. 1990;33(11):1567-1573. Published online November 30, 1990
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Crohn’s disease is a chronic inflammatory disease, which may affect any area of the gastrontestinal
tract from mouth to anus.
The etiology is not clearly defined and rather uncertain. The incidence of the disease is geogra-
phically unequal in world wide distribution. Male and female are equally involved.
We experienced a case of CrohnDisease in 13 year old male child who complained abdominal
pain, anorexia... |
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- Statistical Analysis of Death Cases in Pediatric Ward.
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Kui Ae Jang, Kyeung Bae Park, Jae Ock Park, Chang Hwi Kim, Sang Jhoo Lee
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Clin Exp Pediatr. 1990;33(1):1-9. Published online January 31, 1990
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Statistical analysis of death cases during the 9 years from Jan. 1979 to Dec. 1987 in pediatric ward
of Soonchunhyang university hospital was carried out.
The following results were observed.
1) Total numbers of admission during the 9 years were 16365, of whom 296 expired.
2) Average mortality rate was 1.8% and the annual mortality rate showed decreasing tendency
from 1979 to 1987.
3) In age distribution, the neonates... |
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- Three Cases of Kawasaki Disease Accompanied with Rare Clinical Menifestation.
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Min Yong Oum, Sang Eun Lee, Jae Ock Park, Chang Hwi Kim, Sang Jhoo Lee
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Clin Exp Pediatr. 1989;32(9):1300-1308. Published online September 30, 1989
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We experience 3 cases of Kawasaki disease accompanied with rare clinical manifestations. The
first case was 6 year old boy who accompanied with hydrops of gallbladder and facial palsy. The
second case was 7 month old boy who developed vesicles, crust, and desquamation of the BCG
inoculation site. The third case was 18 month old boy who developed transverse groove (Bow’s line)
of the... |
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- Current Immune Status of Children and Pregnant Women in Korea(I).
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Eun Jung Kim, Ju Kwan Park, Chang Hwi Kim, Sang Jhoo Lee
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Clin Exp Pediatr. 1989;32(5):620-629. Published online May 31, 1989
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This study was conducted to find out rubella immune status as basic data for devising surveillance
plan to prevent rubella epidemic and congenital rubella syndrome in Korea. Rubella ELISA antibody
was tested to the study group of 253 cord blood. 352 children and 486 pregnant women. who visited
Soonchunyhang University Hospital from Feb., 1987 to Oct.. 1987
The provisional results obstanined from the study... |
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- The Precalence and Trend of Obesity in Children and Adolescents.
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Kyu Bum Cho, Soon Bok Park, Sang Chul Park, Dong Hwan Lee, Sang Jhoo Lee, Sung Jae Suh
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Clin Exp Pediatr. 1989;32(5):597-605. Published online May 31, 1989
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The pose of this study is to survey the prevalence and trend of obesity at ages 6 to 11 in Seoul
from 1984 to 1988. The number of children and adolescents comprised of 5,391 boys and 5,289 girls.
Overweight was defined as weight that exceeded the standard weight for height and sex by more than
20% (relaive weight > 120%).
The result was as... |
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- A Case of Type A Niemann-Pick Disease.
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Young Bong Moon, Yang Bin Im, Dong Hwan Lee, Sang Jhoo Lee, In Sook Kim, Tae Jung Kwon, Dong Wha Lee
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Clin Exp Pediatr. 1989;32(3):402-411. Published online March 31, 1989
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We experienced a case of type A Niemann-Pick disease in 31 month-old female infant. She showed
dyspnea, marked hepatosplenomegaly and developmental retardation. Fundoscopic examination
revealed cherry red spots in both macula. Autopsy finding revealed that Iiver, spleen, lung, kidney,
bone marrow, lymph node and brain were involved. Especially multiple ischemic necrosis were found
on cerebral and cerebellar white matter. Generalized muscular atrophy and reticular... |
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- An Epidemiological Study of Bronchial Asthma in Children Who Visited the Emergency Room.
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Ju Kwan park, En Jung Kim, Bok Yang Pyun, Sang Jhoo Lee
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Clin Exp Pediatr. 1989;32(2):215-222. Published online February 28, 1989
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Presently, an increasing incidence of Bronchial asthma in children is of concern to medical
professionals. Worldwide data from surveys indicate a wide range for the prevalence of childhood
asthma, it has been estimated that 5-10% of the young population.
An epidemiological approach was used to test the prevalence of bronchial asthma out of all
pediatric cases referred to the emergency room.
248 cases were selected... |
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- A case of paraquat poisoning in child.
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Min Yong Oum, Sung Ik Cho, Young Chang Kim, Hak Ju Cha, Sang Jhoo Lee
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Clin Exp Pediatr. 1989;32(11):1540-1545. Published online November 30, 1989
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Paraquat is a widely used herbicide and its poisoning in human induces acute renal failure, hepatic
dysfunction, progressive respiratory failure, oral cavity ulcer and cardiac manifestations with high
mortality rate.
We experienced a case of paraquat poisoning in a 12 years old child who revealed acute renal
failure, pneumothorax, subcutaneous emphysema, pneumomediastinum and died 44 hours at acciden-
tal ingestion of paraquat solution inspite of... |
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- A Case of Neonatal Short Bowel Syndrome.
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Gill Hyoun Kim, In Chul Yoo, Dong Hwan Lee, Sang Jhoo Lee
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Clin Exp Pediatr. 1989;32(1):81-86. Published online January 31, 1989
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We experienced a case of neonatal short bowel syndrome due to multiple jejuno-ileal atresia with
microcolon.
On the 1st day of her life, there were symptoms of vomiting and abdominal distension. The
radiological study show multiple dilated intestinalloops and malrotation. On the 4th day of her life,
the extensive enterectomy was done. The remaining small bowel consisted of 30 cm of proximal
jejunum and distal... |
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- Present status and Problems of weaning.
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Young Le Yoon, Moon Hae Bang, Hong Kee Bang, Gang Il Lee, Hak Joo Cha, Jae Ock Park, Sang Jhoo Lee
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Clin Exp Pediatr. 1988;31(7):863-872. Published online July 31, 1988
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This study was conducted to find out the present status and problems of weaning in the provinces
of Korea with the 578 outpatients who visited Chun-An, Ku-Mi and Eum-Sung Soon Chun Hyang
University Hospital from November 1986 to June 1987.
The results and problems obtained from the study are summerized as follows
1) Among 578 parents of this study, 173 were from country and 405... |
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- Clinical Observation of Human Rota Virus(HRV) Gastroenteritis.
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Kee Don Hong, Gil Hyun Kim, Jae Ock Park, Sang Jhoo Lee
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Clin Exp Pediatr. 1988;31(6):700-706. Published online June 30, 1988
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This study was done with the 96 patients with watery diarrhea from Oct. to Nov. 1986.
ELISA study was done to detect Human Rota Virus antigen for all patients. Clinical and laboratory
comparision were made between HRV antigen positive group and HRV antigen negative group.
The results were as follows:
1) HRV antigen was detected in 62 patients (64.6%) among 96 patients of diarrhea or... |
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- Pancreatic ISlet-cell Adenoma in a Neonate.
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Kyu Bum Cho, Yang Bin Im, Dong Hwan Lee, Sang Jhoo Lee, Tae Jeong Kwon, Dong Hwa Lee
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Clin Exp Pediatr. 1988;31(12):1650-1656. Published online December 31, 1988
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Islet cell adenoma is a rare cause of severe neonatal hypoglycemia. A newborn infant with severe
symptomatic hypoglycemia had persistent hypoglycemia in spite of therapy with parenteral glucose
solution.
Islet-cell adenoma of mixed islet-acinar type was found when subtotal pancreatectomy was
performed at 42 days of age. Following surgery she had a transient hyperglycemia and required isulin
for 40 days. She has remained normoglycemic but... |
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- Clinical Evaluation of Bleeding Tendency in Childhood.
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In Chull Yoo, Gill Hyoun Kim, Sang Man Shin, Sang Jhoo Lee
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Clin Exp Pediatr. 1988;31(12):1641-1649. Published online December 31, 1988
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Four hundred and ninety-nine cases of bleeding disorders in childhood who were admitted to
department of pediatrics, Soon Chun Hyang University Hospital during 10 years from July 1977 to
June 1987 were clinically evaluated.
The results obtained were as follows:
1) The incidence of bleeding disorders was 2.97% of total admitted patient. There was no signifi-
cant difference in annual incidence.
2) The peak age of incidence was... |
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- A Case of Medistinal Lipoma.
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Hung Sub Choi, Myung Ho Oh, Chang Hwi Kim, Sang Jhoo Lee, Yong Sik Lee
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Clin Exp Pediatr. 1988;31(1):141-146. Published online January 31, 1988
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The mediastinal lipoma is a rare benign tumor.
Since the original description by Fothergill in 1781, about 120 cases have been reported in literature.
Of these, less than ten have been reported in children below the age of twelve.
We experienced a case of mediastinal lipoma, in a 5 year old girl with mild dry cough. Chest X-ray
showed a large, homogeneous soft tissue... |
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- Diagnosis and Hydrostatic Reduction of 5 Cases of Intussusception Under Ultrasound Guidance.
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Hee Kyung Park, Moon Hae Bang, Jae Ock Park, Sang Jhoo Lee
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Clin Exp Pediatr. 1987;30(8):901-906. Published online August 31, 1987
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I nt ussuscept i on is the condition of invagination of one part of intestinal loop into the contiguous
distal segment. During infancy and early childhood, intussusception is the most common cause of
acquired intestinal obstruction, and it requires emergency treatment.
Recently, the use of ultrasound as a diagnostic and therapeutic tool of intussusception is now
becoming a well-established method because it is simple,... |
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- Present Status and Problems of Weaning.
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Hong Kee Pang, Kyoung Hee Kim, Jae Ock Park, Sang Jhoo Lee
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Clin Exp Pediatr. 1987;30(3):266-274. Published online March 31, 1987
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This study was conducted to find out the present status and problems of weaning in Korea through
the 200 infants who visited Maternal-Child Health Center, Soon Chun Hyang University from Nov.
85 to June 86.
The result and problems obtained from the study are summarized as follows:
1) Most of the infants were under 12 month of age(86.5%).
2) Most of the fathers belonged to 30-39... |
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- A Case of Glanzmann's Thromboasthenia.
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Hee Kyung Park, Kyung Hee Kim, Sang Man Shin, Sang Jhoo Lee
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Clin Exp Pediatr. 1987;30(2):223-228. Published online February 28, 1987
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Glanzmann’s Thromboasthenia is a rare autosomal recessive hemorrhagic disorder characterized
by chronic nonthrombocytopenic purpura, a prolonged bleeding time, and deficient or absent clot
retraction. The major underlying abnormality is defective first phase aggregation of platelets, which
are unresponsive to ADP in any concentration.
The authors experienced one case of Glanzmann’s Thromboasthenia in a 8 year 10 month old
female, who had frequent epistaxis and gingival... |
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- A Clinical Study on Intussusception in Infancy and Childhood.
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Seung Myun Won, Bok Lyun Kim, Jae Ock Park, Sang Jhoo Lee
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Clin Exp Pediatr. 1987;30(2):150-157. Published online February 28, 1987
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Intussusception which is the most common cause of acquired intestinal obstruction during infancy
and early childhood requires emergent diagnosis and treatment because if untreated the infant is
nearly always fatal. A clinical evaluation was performed on 190 cases of intussusception in infants
and children, who were admitted to the Pediatric department of Soon Chun Hyang University
Hospital from Jan. 1979 to Dec. 1983.
The results... |
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- A Clinical Studey on Reye Syndrome.
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Myung Ho Oh, Hung Sub Choi, Chang Hwi Kim, Sang Jhoo Lee
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Clin Exp Pediatr. 1987;30(11):1243-1251. Published online November 30, 1987
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We took clinical study for 47 cases of Reye syndrome at S.C.H. University Hospital during last 8
years from Jan:, 1979 to Dec., 1986.
The results obtained were as follows;
1) There was no significant difference in annual incidence and the seasonal incidence was highest
in sumer and autumn.
2) The sex ratio of male to female was... |
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- Case Report
- A Case of Marfan Syndrom.
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Kyung Hee Kim, Bok Lyun Kim, Chang Hwi Kim, Sang Jhoo Lee
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Clin Exp Pediatr. 1986;29(8):912-917. Published online August 31, 1986
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The Marfan syndrome is a heritable disorder of connective tissue with cardinal manifestations
in the ocular, skeletal and cardiovascular system. We experienced one case of Marfan syndrome
in 13-year-old girl who showed dolichostenomelia, scoiosis, ectopia lentis and mitral valve prolapse.
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- Two Cases of Wilson's Disease.
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Myung Ho Kang, Byoung Tae Kim, Jae Ock Park, Sang Jhoo Lee
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Clin Exp Pediatr. 1986;29(3):336-341. Published online March 31, 1986
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The authors experienced two cases of hepatic from of Wilson* s disease, which diagnosis were confirmed by family history, their characteristic clinical manifestations with hepatic symptoms, Kayser-Fleischer ring and laboratory data with decreased serum ceruloplasmin and copper level and increased urine copper excretion.
Case 1： An 8 8/12 year-old boy with chief complaints of abdominal distension and jaundice showed Kayser-Fleischer ring... |
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- Original Article
- The Clinical Study of Rodenticide Intoxication in Children.
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Song Yee Koh, Myoung Ho Kang, Byoung Tae Kim, Dong Hong Ahn, Sang Jhoo Lee
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Clin Exp Pediatr. 1986;29(3):305-311. Published online March 31, 1986
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A clinical study on 34 cases with rodenticide intoxication seen at Soon Chun Hyang College Hospital from January, 1979 to July, 1984 was performed. The results were as follows:
1) The rodenticide intoxication accounted for 20% of all drug intoxication. Fluoroacetate intoxication 24 cases (70.6%), vacor intoxication 1 cases (2.9%), phosphorus 及 arsenic into xication none and unknown rodenticide intoxication 9 cases... |
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- Case Report
- Partial Trisomy10(q22~q26).
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Hyung Chai Kang, Sung Myun Woh, Dong Whan Lee, Sang Jhoo Lee, Shin Yong Moon
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Clin Exp Pediatr. 1986;29(12):1382-1386. Published online December 31, 1986
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Partial trisomy 10(q22-q26) is a extremely rare chromosomal anomaly.
The authors experienced a case of this syndrome in a female newborn infant. She showed
prominent occiput, flat face, blepharophimosis, hypertelorism, lowset ears, micrognathia,
high-arched palate, simian crease on Lt. palm & overlapping of the 5th finger over the 4th finger,
relatively great big toe, and single umbilical artery.Chromosomal study showed the abnormal
chromosome... |
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- Original Article
- Clinical Observation for Low Birth Infant.
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Kyung Ugk Kim, Man Sik Moon, Song Yee Koh, Dong Whan Lee, Sang Jhoo Lee
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Clin Exp Pediatr. 1986;29(1):18-25. Published online January 31, 1986
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We took clinical observation for low birth weight infant who had been delivered at soon Chun Hyang University Hospital during last 5 years from Jan. 1979 to Dec. 1983. The results obtained were as follows;
1) Incidence of low birth weights was 4.4% and average sex ratio was 1. 24 : 1, of which twin births were 78 cases(15.6%), prematures were... |
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- Case Report
- A Case of Rubinstein-Taybi Syndrome.
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Won Hee Baik, Mee Ran Roh, Young Chang Kim, Hyung Jin Choi, Sang Jhoo Lee
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Clin Exp Pediatr. 1984;27(12):1244-1249. Published online December 31, 1984
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Rubinstein-Taybi syndrome is a new complex of physical findings consisting primarily of
broad thumbs, broad great toes and facial abnormalities, associated with mental retardation.
We have experienced a case of Rubinstein-Taybi syndrome in a 5month-old male infant
who had two recurrent pneumonia a竹acks. The diagnosis was easily established by clinical
features and radiologic examinations.
So a brief review of the pertinent literatures is given.
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- A Case of Congenital Adrenal Agenesis.
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Kyeong Wha Lee, Hyung Jin Choi, Sang Man Shin, Sang Jhoo Lee, Dong Wha Lee
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Clin Exp Pediatr. 1984;27(11):1118-1122. Published online November 30, 1984
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Congenital adrenal agenesis or hypoplasia is very rare disorder which causes adrenal insufficiency.
It is usually the result of an isolated defect of organogenesis. It may be sporadic, or it
may express itself as an autosomal recessive or X-linked disorder within families.
We experienced a baby who revealed hyperpigmentation, hypoglycemia, hyperkalemia and
hyponatremia immediately after birth. Hormone study was compatible with primary adrenal
insufficiency. Complete... |
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- Two Cases of Late Infantile Metachromatic Leukodystrophy.
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Mee Ran Roh, Kyeong Wha Lee, Dong Whan Lee, Sang Jhoo Lee, Dong Wha Lee, Duk Yong Kang, Tae Jung Kwon, Jung Sook Kim
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Clin Exp Pediatr. 1984;27(10):1033-1039. Published online October 31, 1984
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Metachromatic leukodystrophy, a group of progressive degenerative neurologic disease with variable age of onset characterized by an autosomal recessive mode of inheritance, shows an accumulation of the sphingolipid, sulfatide, particularly in the Schwann cell of the central and peripheral nervous system by arysulfatase A deficiency.
2 cases of late infantile metachromatic leukodystrophy are reported, who developed normally during a infantile period,... |
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- Three Cases of Insulin Dependent Diabetes Mellitus in Children.
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Tae Hoon Lee, Sang Chul Park, Chang Hwi Kim, Sang Man Shin, Sang Jhoo Lee
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Clin Exp Pediatr. 1983;26(3):285-289. Published online March 31, 1983
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We experienced three cases of Insulin Dependent Diabetes Mellitus, which revealed fullfilling-
all characteristics of clinical 技 laboratory finding during recent 3 years.
Two diabetic children among three patients had developed diabetic ketoacidosis.
The one of the two cases, 14 aged girl complained of dyspnea & severe emaciation.
The another case, 11 year and 2 month-old boy who had cataract complained of severe
epigastric pain,... |
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- A Case of Dysplastic Kidney and Hydroureter with Distal Treterl Atresia.
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Eun Mi Kim, Jei Hoon Yoo, Dong Whan Lee, Sang Jhoo Lee, Dong Wha Lee, Deuk Yong Kang
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Clin Exp Pediatr. 1983;26(12):1254-1258. Published online December 31, 1983
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We presented a case of dysplastic kidney and Hydroureter with distal ureteral atresia and
reviewed the literatures.
This 5 year old male patient with abdominal mass for 3 years was admitted and took explo-laparotomy.
The diagnosis was confirmed by explo-laparotomy and microscopic finding.
Characteristic microscopic findings of dyaplastic kidney on present case are;
1) Primitive duct, ductules and glomeruli.
2) Duct was lined by cuboidal or columnar... |
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-
- Original Article
- Clinical Study of Hand, Foot, and Mouth Disease and Herpangina.
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Tae Hoon Lee, Jae Ock Park, Chang Hwi Kim, Dong Whan Lee, Sang Man Shin, Sang Jhoo Lee
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Clin Exp Pediatr. 1983;26(1):14-25. Published online January 31, 1983
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A total of 211 children fullfilling all characteristics of Hand, Foot, and Mouth disease (H.F.,& M. Dis.)
and 94 children of Herpangina were studied prospectively during epidemic period of 5 months,
April through August, 1981 in Seoul, Korea.
Maculopapular rash and vesicles that were changed in patterns from time to time were distributed on hands(97%), feet(95%), buttocks(46%), legs(45), arms(16%), trunk (3%),... |
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- Case Report
- Five Cases of Hemorrhagic Disease of Infancy.
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Jung Sook Moon, Eun Hee Koh, Sang Man Shin, Sang Jhoo Lee
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Clin Exp Pediatr. 1982;25(5):518-522. Published online May 31, 1982
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A hemorrhagic disease due to acquired prothrombin complex deficiency is presented in five infants from 3 weeks to 2 months of age. There are 2 cases of intracranial hemorrhage, 1 case of hemothorax, 2 cases of gastrointestinal bleeding, 1 case of epistaxis and 3 cases of petechia, purpura or bleeding from injection site. After the administration of vitamin K, bleeding... |
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- A case of Pierre-Robin Syndrome.
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Soon Ja Han, yeongok bang, Dong Hwan Lee, Sang Jhoo Lee
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Clin Exp Pediatr. 1982;25(4):419-422. Published online April 30, 1982
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Micrognathia, cleft palate and glossoptosis, a combination of anomalies known as Pierre Robin syndrome, causes severe respiratory and alimentary difficulties in affected infants. With appropriate care and treatment, mental development can be made normal. But about 10~25% of children become retarded. We have experienced above case in a female infant, aged 6 months. She was acmitted on account of respiratory... |
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- A Case of Lacunar Skull.
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Eun Hee Koh, Bok Yang Pyun, Dong Whan Lee, Sang Man Shin, Sang Jhoo Lee
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Clin Exp Pediatr. 1982;25(3):300-304. Published online March 31, 1982
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A case of lacunar skull associated with meningomyelocele, spina bifida, kyphcsis on thoracolumbar area, hydrocephalus, bilateral club foot and paralysis of lower extremities at birth was reported. Diagnosis was made by X-ray of skull, whole spine, upper and lower extremities. On skull X-ray film, multiple small area of round rarefaction surrounded by arborizing pattern of bony ridge was visualized on... |
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-
- Original Article
- Statistical Study on Childhood Accidents.
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Hyung Jin Choi, Chang Woo Koh, Sang Man Shin, Sang Jhoo Lee
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Clin Exp Pediatr. 1981;24(9):837-843. Published online September 15, 1981
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Authors reviewed 1809 childhood accident cases who visited the emergency room of Soon Chun hyung Hospital from May, 1974 to Aug. 1980. The following results were obtained; 1. Incidence of accidents was 4.1% of all patients who visited emergency room. 2. The highest age incidence was in the age group of 5-9 years, especially in Falldown, Traffic accident, Laceration accident.... |
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- The Statistical Study on Acute Drug and Chemicals Intoxication in Children.
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Young Chang Kim, Hyung Jin Choi, Jae Ock Park, Dong Whan Lee, Sang Jhoo Lee
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Clin Exp Pediatr. 1981;24(8):760-765. Published online August 15, 1981
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A statistical study on 135 cases of acute poisoning who were treated in Pediatric department of Soon Chun Hyang College Hospital from May, 1974 to August, 1980 was performed. The results are as follows: 1. Seasonal incidence was more prevalent in summer. (from June to August, Table 2) 2. It occurred more frequently in male than female and high incidence... |
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- Clinical Obseervation of 12 cases of Kawasaki Disease.
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Bok Yang Pyun, Chang Woo Koh, Dong Whan Lee, Sang Jhoo Lee
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Clin Exp Pediatr. 1981;24(3):245-256. Published online March 15, 1981
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Kawasaki Disease of Mucocutaneous Lymph Node Syndrome, first described by Kawasaki in 1967, is an acute febrile disease of unknown etiology. Until recently, more than 17,000 cases of this disease have been listed in the survey of a special study group supported by the Japanese Ministry of Health and Welfare. And a number of cases have been reported even outside... |
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- Case Report
- A Case of Staphylococcal Scalded Skin Syndrome.
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Jung Sook Moon, Soo Ok Lee, Dong Hwan Lee, Sang Jhoo Lee
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Clin Exp Pediatr. 1981;24(2):169-172. Published online February 15, 1981
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The authors experienced a case of staphylococcal scalded skin syndrome in 6 month old male infant and reported with brief review of literatures. His chief complaints on admission were fever, vomiting, and watery diarrhea for one day. On the fourth hospitalization day, generalized erythema was developed which was followed by generalized skin exfoliation and methicillin therapy was started. On the... |
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-
- Original Article
- Clinical and Statistical Observation for Low Birth Weight Infants.
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Chong Ok Lee, Eun Hee Koh, Sang Man Sin, Sang Jhoo Lee
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Clin Exp Pediatr. 1981;24(12):1142-1148. Published online December 15, 1981
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A clinical and statistical observation was made on 383 low birth weight infants, delivered at Soon Chun Hyang hospital from Jan. 1st 1975 to May 31st 1980. The results were as follows: 1)Incidence of low birth weight infants was 5. 3% without sexual predominence, of which twin births were 13.3%, prematures were 78.3%, SGA were 26%.
2) Maternal predisposing factors of low... |
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- Case Report
- A Case of Cushingoid syndrome Associated with Mediastinal Lipomatosis, Aseptic Necrosis of Hip Joint and Growth Retardation.
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Chang Woo Koh, Hyung Jin Choi, Chang Hwi Kim, Sang Man Shin, Sang Jhoo Lee
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Clin Exp Pediatr. 1981;24(10):973-981. Published online October 15, 1981
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The 15 year-old female patient was admitted with the complaints of moon face, obesity and short stature. She has received steroid therapy since 11 years ago at home to control joint pain due to rheumatoid arthritis. The diagnosis was confirmed by history of long-term steroid therapy, characteristic clinical features, biochemical studies and radiological studies. In radiological studies, superior mediastinal widening,... |
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- A Case of Diabetes Insipidus associated with Suprasellar Germinoma.
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Soo Ok Lee, Hye Yung Hwang, Woo Hyun, Sang Jhoo Lee, Dong Wha Lee
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Clin Exp Pediatr. 1980;23(12):1048-1053. Published online December 15, 1980
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We report I case of diabetes insipidus associated with suprasellar germinoma, obstructive hydrocephalus and both optic nerve atrophy. In this patient, symptoms of increased intracranial pressure was preceded by characteristic polyuria and polydipsia. The water restriction and pitressin test resulted in central originated diabetes insipidus. Computerized tomography in the brain revealed smooth marginated rounded mass density measuring 3.9 cm obliterating... |
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- A Case Report of Congenital Ileal Atresia with Microcolon.
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Eun Kim, Hye Young Hwang, Dong Hwan Lee, Sang Jhoo Lee
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Clin Exp Pediatr. 1979;22(9):809-813. Published online September 15, 1979
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This is a case report of the congenital ileal atresia with disuse microcolon. The patient was a 3 day-old male newborn infant who was admitted in department of pediatrics Soon Chun Hyang Hospital with complaints of persistant vomitings, no meconium passage, and jaundice from a few hours after birth. The diagnosis was established by characteristic clinical features and barium enuma... |
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- A Case of Athyrotic Cretinism.
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Jae Ock Park, Eun Kim, Woo Hyun, Sang Jhoo Lee
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Clin Exp Pediatr. 1979;22(7):556-560. Published online July 15, 1979
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We experienced a case of athyrotic cretinism in a 9 month old female patient. She had a history of prolonged jaundice in neonatal period. The physical findings that suggest she had hypothyroidism were large anterior fortanel, unbilical hernia, widely separated suture line of the skull, large and protruded tongue, eyelid edema, no eruption of any tooth and skin change. X-ray... |
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-
- Original Article
- A Clinical Study on Intussusception in Infancy and Children.
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Jae Ock Park, Soo Ok Lee, Woo Hyun, Sang Jhoo Lee
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Clin Exp Pediatr. 1979;22(4):292-299. Published online April 15, 1979
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A retrospective clinical study on 63 cases of intussusception in infants and children, who were admitted to the department of pediatrics and surgery from May, 1974 to Feb. 1978, was done. The prognosis of this disease is dependent upon early diagnosis and treatment but the causatio of this disease is not clear yet. It is a relatively common disease and... |
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- Case Report
- Two Cases of Kasabach-Merritt Syndrome.
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Hye Yong Hwang, Eun Kim, Jae Ock Park, Dong Hwan Lee, Sang Jhoo Lee
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Clin Exp Pediatr. 1979;22(12):1067-1073. Published online December 15, 1979
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Kasabach-Merritt syndrome is rare disorder which consists of hemangioma and thromobocytopenia occurring in infatns. Two cases of giant hemanioma with thrombocytopenia and anemia are reported with review of literures. It is postulated that the abnormalities resulted from intravascular coagulation within the hemangioma. Those patients were managed with prednisolone administration, blood transfusion and compression with the elastic bandage over the hemangioma.... |
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-
- Original Article
- Two Cases of Duchenne Type of Muscular Dystrophy in Sisters
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Soo Ha Park, Eui Hyun Jo, Sang Man Shin, Sang Jhoo Lee, Moon Ho Yang
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Clin Exp Pediatr. 1974;17(9):607-612. Published online September 30, 1974
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Authors has experienced two cases of Duchenne type of muscular dystrophy in 8 years old
female child and in her 2 years old sister.
Initial symptoms were frequent fall and waddling gait in these two cases which has began to
develop at the age of 4 years in elder sister and at the age of 2 years in younger sister.
Diagnosis has confirmed by... |
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- Case Report
- A Case of Erythroleukemia in Childhood
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Eui Hyun Jo, Sang Man Shin, Sang Jhoo Lee, Myong Joon Cho
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Clin Exp Pediatr. 1974;17(4):307-311. Published online April 30, 1974
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A case of erythroleukemia in 8 year old boy is presented. It is a systemic hemopathy characterized
by abnormal proliferation of defective erythroid and myeloid cells and is rare in childhood.
Physical examination shows pallor, general weakness and necrotic inflammation in mucous
membrane of mouth, tonsils and gingivae associated with bleeding, there are grade 11-111 systolic
murmur on apical area, hepatosplenomegaly and a few... |
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- An Autopsy Case of Congenital Jejunal Atresia
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Soo Ha Park, Sang Man Shin, Sang Jhoo Lee, In Keun Bae, Hoong Zae Joo, Moon Ho Yang
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Clin Exp Pediatr. 1974;17(2):144-148. Published online February 28, 1974
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This is an autopsy case of congenital jejunal atresia in an 11-hour-old male newborn infant who
was admitted to pediatric ward because of bile stained vomitus, abdominal distention and no passage
of meconium stools.
End to side jejunioleostomy has carried out on 2nd hospital day and expired on 6th hospital day.
The site of atresia was in distal portion of the jejunum which was... |
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- A Case of Klippel-Trenaunay-Weber Syndrome
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Jin Yung Ro, Eui Hyun Jo, Sang Man Shin, Sang Jhoo Lee, Tai Yun Yoo
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Clin Exp Pediatr. 1973;16(12):960-964. Published online December 31, 1973
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A case of Klippel-Trenaunay-Weber syndrome with macrodactylia in a 11-year-old boy is presented who was admitted to our Kyung Hee Medical Center with Chief complaints of nevus flammeus, swelling of the left lower leg and foot for 3 years duration. This patient was born with an extensive nevus flammeus of left leg, left upper arm, abdomen and right lumbar region.... |
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- Case Report
- A Case of Duodenal Stenosis Associated with Down’s Syndrome
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Jin Yung Ro, Eui Hyun Jo, Dong Won Chun, Sang Jhoo Lee
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Clin Exp Pediatr. 1973;16(10):758-762. Published online October 31, 1973
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We had a case of severe duodenal stenosis associated with Down’s syndrome, a 3 day old female infant who was admitted to our Kyung Hee Medical Center with chief compliant of projectile vomiting and fever. On physical examination she had a typical monogloid appearance such as small head (circum. 29 cm) and head is flattened anteriorly and posteriorly, prominant epicanthal... |
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- A Case of Debre-Semelaigne Syndrome
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Eui Hyun Jo, Jin Yung Ro, Dong Won Chun, Sang Jhoo Lee
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Clin Exp Pediatr. 1973;16(10):787-793. Published online October 31, 1973
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A case of Debre-Semelaigne syndrome, hypothyroidism with muscular hypertrophy, was presented. 4 year and 2 month old male patient was admitted with retarded growth, mental retardation, general muscular hypertrophy and muscular hypertonia. Thyroid function test revealed hypofunction and no visualization of thyroid gland was demons
trated by scintiscan. Bone X-ray study showed retarded bone growth. Muscle biopsy from calf muscle showed... |
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- Original Article
- The Clinical Statistical observation of Congenital Syphilis
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Buem Soo Roh, Kyung Ja Lee, Yong II Lee, Sang Jhoo Lee
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Clin Exp Pediatr. 1971;14(3):175-180. Published online March 31, 1971
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The authors observed 31 cases of congenital syphilis in the newborn and infants treated at pediatric ward of Han-Il Hospital during the period from Jan. 1965 to Feb. 1671. The results are as follows. 1)The number of patients was 31 cases, 23 in male and 8 in female. 2)The incidence of congenital syphilis in the newborn infants who were delivered... |
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- Methemoglobinemia
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Young Shik Hong, Jong Hyuk Kee, Yong IL Lee, Sang Jhoo Lee
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Clin Exp Pediatr. 1970;13(3):159-164. Published online March 31, 1970
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A case of a cyanotic, 7 years old boy who had no cardiac, pulmorrary, or neurological disease is described.
He was admitted to Ped. ward, Han-11 Hosp, on May 2, 1969 because of generalized cyanosis, headache and joint pain. The cyanosis was remarkable on lips, cheeks, fingers, toes and oral mucosa. This cyanosis proved to be due to the presence in... |
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- Statistical Studies on Acute Glomerulonephritis in Children
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Yung Kak Song, Chui Kyu Kim, Young Il Lee, Sang Jhoo Lee
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Clin Exp Pediatr. 1969;12(8):423-430. Published online August 31, 1969
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During the last 7 years 131 cases of acute glomerulonephritis were admitted to Dep. of Ped. Han II Hospital and evaluated statistically. The resutlts were as follows. 1)The sex incidence was slightly higher in boys than in girls and the ratio was 2. 6 : 1. The age incidence was highest in the age of 7 to 9. Seasonal peak... |
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- Case Report
- A Case Repm't of Incomplete Duodenal Obstruction due to Malrotation of Intestine
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Jong Hyuk Lee, Yong Kil Lee, Yong II Lee, Sang Jhoo Lee, Wha Yung Lee
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Clin Exp Pediatr. 1969;12(4):217-220. Published online April 30, 1969
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A 3 months old Korean male was admitted to dept, of Pediatrics, Han-il Hospital because of projectile vomiting and visualized peristaltic waves on July 28, 1968. Since 4 days after birth, bile-stained vomiting was occurred immediately after every feeding for 6 days in spite of sufficient evacuation of swallowed air and progressively aggravated. At this time, vomiting was com trolled... |
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- An Autopsy Case of Situs Inversus Viscerum Totalis
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Kyung Ja Lee, Jong Hyuk Lee, Yong Kil Lee, Sang Jhoo Lee, Je G. Chi, Geung Hwan Ahn
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Clin Exp Pediatr. 1969;12(12):715-720. Published online December 31, 1969
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An 2. 7 kg weighing male baby was born with a large pedunculated mass in the occipital area of the head. The baby expired on 21st day after birth, due probably to infected cephalocele with diarrheal disorder. Postmortem examination revealed the following: All thoraco-abdominal viscera and vessels were in the mirror-image position of the normal. The heart was in the... |
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- Original Article
- Observation of C-Reactive Protein in Maternal and Neonatal Sera
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Chui Kyu Kim, Dong Won Chun, Byung Youn Lee, Sang Jhoo Lee, Han Woong Choi
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Clin Exp Pediatr. 1969;12(1):21-24. Published online January 31, 1969
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From our study of sera of 30 parturient women and their normal full-term newborn infants, the following observations are noted. 1.A positive C-reactive protein titer was found in 20% pregnant women. All of the cord blood specimen were negative for this reaction. There would appear to be no transferral of C-reactive protein across the placental membrane. 2.The incidence of positive... |
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- Case Report
- A Case of Sublingual Ectopic Thyroid
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Chang Hyup Kim, Jae Hak Seo, Chui Kyu Kim, Sang Jhoo Lee
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Clin Exp Pediatr. 1968;11(3):149-154. Published online March 31, 1968
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A case of sublingual ectopic thyroid was reported. An 8 year and 6 month old boy had retarded bone developement, delayed teeth eruption and ectopic thyroid was demonstrated by scintigram. Thyroid scintigram revealed ectopic thyroid which located on slightly left side under the tongue connected with thyroid gland.
Patient had been on desiccated thyroid and doing well now. Review of literature... |
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- Two Cases of Spontaneous Fractures in Miliary Tuberculosis and Tuberculous Meningitis
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Chang Hyup Kim, Jong Hyuck Lee, Kyung Ja Lee, Sang Jhoo Lee
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Clin Exp Pediatr. 1968;11(2):91-94. Published online February 28, 1968
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Only few cases describing spontaneous fractures in tuberculous meningitis were reported in the literatures. Recently, we experienced two such cases, who daring their treatment for miliary tuberculosis and tuberculous meningitis developed spontaneous fractures of the lower extremities. Case 1: A 3 year and 4 month old Korean boy was admitted to Hanil Hospital on September 8,1966, with chief complaints of... |
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- A Case Report of the Successful Treatment of Acute Renal Failure by the Peritoneal Dialysis
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Yong Kil Lee, Dong Won Chun, Sang Jhoo Lee
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Clin Exp Pediatr. 1968;11(12):657-662. Published online December 31, 1968
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A 8 years 5 month old boy was admitted to Ped. Dept, of Han-IL Hospital because of generalized edema, oliguria with macroscopic hematuria, nausea and vomiting on Dec. 7, 1967. Above mentioned symptoms had been developed since 2 days before admission. 2 weeks prior to the onset, patient was afflicted with scarlet fever.
On admission, physical examinations revealed branny skin desquamation... |
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- Original Article
- Clinical and Bacteriological Observation in Cases with Neonatal Septicemia
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Byung Youn Lee, Yong II Lee, Sang Jhoo Lee, Han Woong Choi
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Clin Exp Pediatr. 1966;9(2):61-69. Published online March 31, 1966
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Clinical and bacteriological observation in cases with neonatal septicemia were carried out in the pediatric ward of Han-11 Hospital during the period from October 1962 to September 1965. During the study period, a total 41 patients were experienced and the diseas was characterized as commonly affecting the smaller infants and the male child. Gastrointestinal syipptoms, jaundice and respiratory symptoms were... |
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- Studies on Hemolytic Streptococcal Infections in Korean
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Sang Jhoo Lee
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Clin Exp Pediatr. 1964;7(5):155-173. Published online December 31, 1964
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The Laneefield group A hemolytic streptococcus liberates, among other substances, a hemolyzing agent
or streptolysin. Todd identified a streptolysin S and a much more antigenic streptolysin O. The antibody
for streptolysin O (ASO) is readily measurable, and a specific antibody of the hemolytic streptococcus and
according to Mote and Jones, is not increased in infection in which the streptococcus has been excluded.
A rise... |
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- Case Report
- A case with Progressive Muscular Dystrophy
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Yong II Lee, Byong Yoon Lee, Sang Jhoo Lee
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Clin Exp Pediatr. 1964;7(4):151-153. Published online November 30, 1964
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A twelve years and five months old boy was admitted to the Hanil Hospital on August 17, 1964 because of limping and muscular weakness. He was normal full term spontaneous delivery. No family incidence of this disease was detectable. Father was afflicted with gonorrhea or other venereal disease several times and mother has contracted pulmonary tuberculosis four years ago. The... |
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