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Original Article
A Clinical Study on Intussusception in Infancy and Childhood.
Seung Myun Won, Bok Lyun Kim, Jae Ock Park, Sang Jhoo Lee
Clin Exp Pediatr. 1987;30(2):150-157.   Published online February 28, 1987
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...
Case Report
Partial Trisomy10(q22~q26).
Hyung Chai Kang, Sung Myun Woh, Dong Whan Lee, Sang Jhoo Lee, Shin Yong Moon
Clin Exp Pediatr. 1986;29(12):1382-1386.   Published online December 31, 1986
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...
A Case of Marfan Syndrom.
Kyung Hee Kim, Bok Lyun Kim, Chang Hwi Kim, Sang Jhoo Lee
Clin Exp Pediatr. 1986;29(8):912-917.   Published online August 31, 1986
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.
Two Cases of Wilson's Disease.
Myung Ho Kang, Byoung Tae Kim, Jae Ock Park, Sang Jhoo Lee
Clin Exp Pediatr. 1986;29(3):336-341.   Published online March 31, 1986
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...
Original Article
The Clinical Study of Rodenticide Intoxication in Children.
Song Yee Koh, Myoung Ho Kang, Byoung Tae Kim, Dong Hong Ahn, Sang Jhoo Lee
Clin Exp Pediatr. 1986;29(3):305-311.   Published online March 31, 1986
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...
Clinical Observation for Low Birth Infant.
Kyung Ugk Kim, Man Sik Moon, Song Yee Koh, Dong Whan Lee, Sang Jhoo Lee
Clin Exp Pediatr. 1986;29(1):18-25.   Published online January 31, 1986
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...
Case Report
A Case of Rubinstein-Taybi Syndrome.
Won Hee Baik, Mee Ran Roh, Young Chang Kim, Hyung Jin Choi, Sang Jhoo Lee
Clin Exp Pediatr. 1984;27(12):1244-1249.   Published online December 31, 1984
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.
A Case of Congenital Adrenal Agenesis.
Kyeong Wha Lee, Hyung Jin Choi, Sang Man Shin, Sang Jhoo Lee, Dong Wha Lee
Clin Exp Pediatr. 1984;27(11):1118-1122.   Published online November 30, 1984
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...
Two Cases of Late Infantile Metachromatic Leukodystrophy.
Mee Ran Roh, Kyeong Wha Lee, Dong Whan Lee, Sang Jhoo Lee, Dong Wha Lee, Duk Yong Kang, Tae Jung Kwon, Jung Sook Kim
Clin Exp Pediatr. 1984;27(10):1033-1039.   Published online October 31, 1984
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,...
A Case of Dysplastic Kidney and Hydroureter with Distal Treterl Atresia.
Eun Mi Kim, Jei Hoon Yoo, Dong Whan Lee, Sang Jhoo Lee, Dong Wha Lee, Deuk Yong Kang
Clin Exp Pediatr. 1983;26(12):1254-1258.   Published online December 31, 1983
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...
Three Cases of Insulin Dependent Diabetes Mellitus in Children.
Tae Hoon Lee, Sang Chul Park, Chang Hwi Kim, Sang Man Shin, Sang Jhoo Lee
Clin Exp Pediatr. 1983;26(3):285-289.   Published online March 31, 1983
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,...
Original Article
Clinical Study of Hand, Foot, and Mouth Disease and Herpangina.
Tae Hoon Lee, Jae Ock Park, Chang Hwi Kim, Dong Whan Lee, Sang Man Shin, Sang Jhoo Lee
Clin Exp Pediatr. 1983;26(1):14-25.   Published online January 31, 1983
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%),...
Case Report
Five Cases of Hemorrhagic Disease of Infancy.
Jung Sook Moon, Eun Hee Koh, Sang Man Shin, Sang Jhoo Lee
Clin Exp Pediatr. 1982;25(5):518-522.   Published online May 31, 1982
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...
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 Lacunar Skull.
Eun Hee Koh, Bok Yang Pyun, Dong Whan Lee, Sang Man Shin, Sang Jhoo Lee
Clin Exp Pediatr. 1982;25(3):300-304.   Published online March 31, 1982
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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