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Case Report
One Case of 13q-Syndrome.
C O Lee, T H Lee, D W Lee, S J Lee, D.W Lee, D.Y Kang, K.Y Choi, Je G Ghi
Clin Exp Pediatr. 1982;25(7):743-747.   Published online July 31, 1982
13 q-syndrome based on loss of specific band was first described by Bain and Gauld in 1963 and may be transmitted if one parents is translocation carrier. We experienced one case of 13p-syndrome with ercephalocele in newborn diagnosed by clinical feature, chromosomal study and autopsy findings. He had multiple anomalies such as microcephaly, hypertelorism, microphthalmia, absent thumbs, clinodactyly, equinovarus, bifid...
Sonography in the Diagnosis and Management of Hydrops of the Gallbladder in Childern with Mucocutaneous Lymph Node Syndrome.
Byung Lyul Lee, Byung Hwan Lee, Kwang Chan Doh, Sung Il Ahn
Clin Exp Pediatr. 1982;25(6):633-637.   Published online June 30, 1982
Acute hydrops of the gallbladder is described in one patient who had mucocutaneous lymph node syndrome. During the course of her illness, acute addominal pain, vomiting and right upper guadrant tenderness were developed. Diagnosis was readily made with ultrasonography, and the patient was followed with this te-chnique. We managed her conventionally without surgical intervention. The galbladder returned to normal size...
Hyperviscosity Syndrome in Newborn.
Yong Soon Kim, Sook Hee Lee, Ja Hoon Koo, Doo Hong Ahn
Clin Exp Pediatr. 1982;25(6):622-627.   Published online June 30, 1982
We experienced Hyperviscosity syndrome in 5 newborn infants during 6 months period from August 1980 to January 1981. Diagnosis was made on the basis of characteristic clinical symp-toms along with polythemia. The following results were obtained. Sex in 5 affected infants showed male in 2 and female in 3. And gestational age showed preterm in 3 and full term in...
Two Cases of Postvaricella Reye Syndrome.
Won A Park, Sang Keun Chi, In Ho Kim, Churl Young Chung
Clin Exp Pediatr. 1982;25(5):528-532.   Published online May 31, 1982
Authors observed two cases of Reye syndrome in 7 and 8 year old male patients who had begun to vomit after chickenpox. The interval between the onset of varicella rash and encephalopathy of Reye syndrome was 4 days in both these cases. The initial laboratory findings revealed increased serum transaminase and blood ammonia levels which returned to normal on 18...
A case of Pierre-Robin Syndrome.
Soon Ja Han, yeongok bang, Dong Hwan Lee, Sang Jhoo Lee
Clin Exp Pediatr. 1982;25(4):419-422.   Published online April 30, 1982
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...
A Case of Hypereosinophilic Syndrome.
Chul Young Lee, Ki Sup Chung, Byung Soo Kim, Chang Jin Kim, Chan Il Park
Clin Exp Pediatr. 1982;25(4):388-392.   Published online April 30, 1982
Marked eosinophilia is a common finding in many disease, occurring most frequently in allergic and parasitic conditions. A Separate syndrome characterized by peripheral eosinophilia and multisystem eosinophilic infiltration has been reported by many authors with a variety of diagnoses. In 1968, Hardy and Anderson proposed the term hypereosinophilic syndrome to encompass the entire group and in 1975, Chusid reported 14...
Original Article
Clinical Diagnostic Application of Serum Cholinesterase.
Kyu Cha Kim
Clin Exp Pediatr. 1982;25(3):258-268.   Published online March 31, 1982
Serum cholinesterase and other commonly employed function tests were determined in 12 patients with nephrotic syndrome, 17 patients with infectious hepatitis and 7 patients with acute glomerulonephritis who were available for se5rial studies the evaluation of which was helpful in diagnosis, management and prognosis of various disease. The results were as follows. 1) Serum cholinesterase activity in patients with nephrotic...
Case Report
A case of Finnish Type of Congenital Nephrotic Syndrome.
Jeong Sik Min, Yang Kook Shon, Soo Woong Lee, Suk Chul Kang, Yong Koo Park, Moon Ho Yang
Clin Exp Pediatr. 1982;25(2):175-182.   Published online February 28, 1982
The Finnish type of Congenital Nephrotic Syndrome is characterized by large placenta, early manifestation, growth and developmental delay and resistance to treatment. Authors experienced a case of characteristic Finnish type of Congenital Nephrotic Syndrome in a girl, who was admitted to the Pediatric Department of KHUH at 2 1/1 months of age because of generalized edema and abdominal distension and...
A Case of Trisomy Syndrome.
Keun Chul Choi, Hae Jung Cho, Que Sang Lee, Myung Ho Lee
Clin Exp Pediatr. 1982;25(1):102-106.   Published online January 31, 1982
We have seen a case of Edward syndrome in a new born neonate who was born at local obstetrics clinics to a healthy 27 years old mother. Just after birth, she was transfered to us and brought to emergency room, because of dyspnea and abnormal apperance, characterized by prominent occiput low set malformed ear, micrognathia, webbed neck, short sternum, small...
The Kocher-Debre-Semelaigne Syndrome.
M Y Chung, S I Kwon, S J Lee, D H Kum
Clin Exp Pediatr. 1982;25(1):92-96.   Published online January 31, 1982
A 4-year old girl with the Kocher-Debre-Semelaigne syndrome, hypothyroidism with generalized muscular hypertrophy is described. Histologic examination of a calf muscle showed musclular hypertrophy with focal eosinophilic degeneration. The stigmas of hypothyroidism and the muscular hypertrophy disappeared promptly and concomitantly following therapy with desiccated thyroid. Similar cases reported in literature are briefly reviewed. The clinical and histologic changes of the...
A Case of Sturge-Weber Syndrome.
Soo Young Kim, Hyang Sook Kim, Myung Sook Kim, So Young Park, Dong Hak Shin
Clin Exp Pediatr. 1981;24(11):1111-1115.   Published online November 15, 1981
Recently, we experienced a case of Sturge-Weber Syndrome in a 9 month old female. The diagnosis was established by typical clinical features of Sturge-Weber Syndrome in eluding facial portwine nevus, convulsion, left hemiparesis, glaucoma and typical calcification & brain atrophy as seen on on the brain CAT. Plain radiolographys of the skull revealed no evidence of calcification, while the brain...
A Case of Marfan's Syndrome.
Ki Hyun Yoon, Jung Suh Suh, Son Sang Suh, Jong Woo Shin
Clin Exp Pediatr. 1981;24(11):1106-1110.   Published online November 15, 1981
We have experinced a case of Marfan’s syndrome'in 27 months old female children. Marfan's syndrome is characterized by skeletal, ocular and cardiovascular abnormalities. Diagnosis was established by clinical characteristics with radiologic and laboratory findings. Pertiment literatures on Marfan’s syndrome also reviewed briefly.
A Case of Cushingoid syndrome Associated with Mediastinal Lipomatosis, Aseptic Necrosis of Hip Joint and Growth Retardation.
Chang Woo Koh, Hyung Jin Choi, Chang Hwi Kim, Sang Man Shin, Sang Jhoo Lee
Clin Exp Pediatr. 1981;24(10):973-981.   Published online October 15, 1981
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,...
A Case of D1-Trisomy Syndrome.
Soon Hee Choi, Seung Joo Lee, Keun Lee
Clin Exp Pediatr. 1981;24(10):968-972.   Published online October 15, 1981
One cases of D1-Trisomy Syndrome which was confirmed by chromosome study at Ewha Womans University Hospital is presented. The premature female infant was delivered spontaneously at 36 1/2 weeks of gestation at Ewha Womans University. The family and antenatal history were not remarkable except ingestion of some kinds of antibiotics and anti-inflammatory drugs during the first trimester. On physical examination...
Mucocutaneous Lymph Node Syndrome: Report of one case complicated by gallbladder hydrops and diagnosed by ultrasound.
Chul Ho Lee, Sung Won Park, Chang Soo Han, Soon Jai Lee, Yeun Ki Kim
Clin Exp Pediatr. 1981;24(9):877-881.   Published online September 15, 1981
A female patient with mucocutaneous lymph node syndrome is presented. During the course of her illness, she developed acute abdominal pain secondary to hydrops of gallbladder. The diagnosis was facilltated by ultrasound. We managed her conventionally without surgical intervention. It is interesting that the age of patients complicated by gallbladder hydrops is high compared with the age frequency of MCLS....
Original Article
Cluster of Guillain-Barre Syndrome.
Young Mo Sohn, Sung Sik Lee, Kwan Sub Chung, Ki Sub Chung, Seung Kyu Lee, Pyung Kil Kim, Kir Young Kim, Duk Jin Yun, Kyoung Ja Cho
Clin Exp Pediatr. 1981;24(9):820-825.   Published online September 15, 1981
Of 7 cases of Guillain-Barre syndrome reviewed, which was admitted to the Department of Pediatrics Yonsei University, College of Medicine during 3 months period from July through September 1980, serologic surveys for an infectious agent were found to be without demonstrable causes such as cytomegalovirus and measles virus. We reviewed 87 acses of Guillain-Barre syndrome, which was admitted to our...
Case Report
A Case of Beckwith Syndrome.
Kyung Tae Kim, Dae Sik Hong, Byung Do Nam, Kew Taek Kim
Clin Exp Pediatr. 1981;24(7):696-698.   Published online July 15, 1981
We experienced one case of Beckwith syndrome. This one day aged male neonate manifested macroglossia, umbilical hernia, visceromegaly, hypoglycemia, gigantism and polycythemia. A brief review of related literature is also presented.
Original Article
Diagnostic Value of Serum Immunoglobulins in Glomerulonephritis.
Pyung Kil Kim, Kyo Sun Kim, Chul Lee, Nan Ae Kim, Jae Seung Lee
Clin Exp Pediatr. 1981;24(7):652-658.   Published online July 15, 1981
Serum immunoglobulin concenatrations were measured in 156 patients with various types of glomerulonephritis such as acute poststreptococcal glomerulonephritis, minimal lesion nephrotic syndrome and Henoch-Sch?lein purpura nephritis. 1) Serum IgG level was above normal mean in acute poststreptococcal glomerulonephritis, and normal range in Henoch-Scholein purpura nephritis. Serum IgG concentrations were significantly reduced in minimal lesion nephrotic syndrome. 2) Serum IgA concentrations...
Clinical Study on Idiopathic Nephrotic Syndromein Children.
Haeng Mi Kim, Chang Ho Lee, Ja Hoon Koo, Doo Hong Ahn
Clin Exp Pediatr. 1981;24(6):549-558.   Published online June 15, 1981
A clinical observation was done on 38 children with idiopathic nephrotic syndrome, who had been admitted to our pediatric department during past 3 years period, from January 1978 to September 1980. The following results were obtained: At the beginning of illness, 42% were in the age group of 3~7year, and male to female ratio was approximately 3:1 of male preponderance....
Form Stability Test on Gastric Aspirate and Respiratory Distress Syndrome in Newborn Baby.
Byung Do Nam
Clin Exp Pediatr. 1981;24(5):437-444.   Published online May 15, 1981
Form stability test on gastric aspirate was performed on 102 cases of newborn within 30 minutes afterbirth, who were admitted to Special Care Unit of St. Benedict Hospital from Sep. 1977 to Aug. 1979, and following results were obtained. 1) There was no differnce between amniotic fluid and gastric aspirate in control group. 2) In all newborn infants with positive...
Case Report
Recurrent Guillain-Barr'e Syndrome.
Kyo Sun Kim, Jae Song Kim, Pyung Kil Kim
Clin Exp Pediatr. 1981;24(4):367-450.   Published online April 15, 1981
This paper presents a case of^recurrent Guillain-Barre syndrome in a 13 year-old boy. Recu-rrent rate is variable but almost all of the authors expressed it was very rare and some of them recurred more than two times and and its interval also variable from few months to 17 years. In our case, he developed a typical ascending, symmetric motor paralysis...
Hepatorenal Syndrome.
Kyo Sun Kim, Young Mo Sohn, Jung Soo Kim, Jae Seung Lee, Pyung Kil Kim, Tae Jung Kwon, In Jun Choi
Clin Exp Pediatr. 1981;24(3):257-270.   Published online March 15, 1981
Hepatorenal syndrome is generally urged, at least until specific interrelationships between the two organs are confirmed by experimental and clinical data. Case I was a 11 year old boy, who had been suffered from acute fulminant viral hepatitis, which had developed acute hepatic necrosis associated with acute renal failure. Cass H was a 10 year old girl, who was performed corrective...
A case of Congenital Syphilitic Nephrotic Syndrome.
H S Kim, S K Park, D H Shin
Clin Exp Pediatr. 1981;24(1):94-99.   Published online January 15, 1981
We have experienced a case of congenital syphilitic nephrotic syndrome in a 4 months old boy, who was admitted to presbyterian hospital, Daegu, Korea. He was sucessfully treated with penicillin of 2 weeks duration. We made brief review of the related literatures.
A Case of Cushing's Syndrome Associatied with Hypertensive Encephalopathy.
Choong Rae Kim, In Soon Park, Do Seung Lee, Jae Sun Park, Kee Ryo Chang, Soon Yong Lee
Clin Exp Pediatr. 1981;24(1):80-84.   Published online January 15, 1981
A 8-yrs-old boy was admitted because of convulsion and coma. The diagnosis of Cushing's syndrome(key word) associated with hypertensive encephalopathy(key word) due to right adrenocortical carcinoma(key word) was made by clinical features, biochemical studies, radiological studies and pathological examination. The tumor was successfully resected by right adrenalectomy. But 22 months later after operation, he died of dyspnea and heart failure....
Original Article
Effect of the Glucocorticoids on the Vertebral Bone Density in Children with the Nephrotic Syndrome
Jong Young Kim, Yong Hoon Park
Clin Exp Pediatr. 1955;38(7):946-954.
Purpose : This study was conducted to evaluate that long term glucocorticoid treatment in children with the nephrotic syndrome can produce a significant loss of bone mass by measuring of bone mineral density(BMD) Methods : We measured BMD at lumbar vertebra(L2-L4) using dual enegy X-ray absorptiom-etry in 36 patients with the nephrotic syndrome who were administered prednisolone over 6 months and...
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