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Case Report
A 18 Trigomy syndrome, Probably Combined with DiGeorge Syndrome.
Wi In Kang, Heung Jae Lee, Chong Moo Park
Clin Exp Pediatr. 1980;23(2):143-148.   Published online February 15, 1980
A case of 18 trisomy syndrome in a newborn female infant was presented with a brief review of literatures. She was characterized by low brith weight, swallowing difficulty, cleftplate and lip, malformed ears, low hair line, occipital prominence, large atd angle, club feet, adduction deformity of limbs, absence of thymus shadow in a film of chest, and P.D.A. On the...
A case of Twin to twin Transfusion Syndrome.
Heak Sang Kwan, Heung Jae Lee, Soo Jee Moon, Soon Yong Lee
Clin Exp Pediatr. 1979;22(12):1087-1090.   Published online December 15, 1979
A case of twin to twin transfusion syndrome is reported. These babies were disclosed severe anemia in one twin and intense plethora in another one. The different appearence was coincided with hematologic results. So, anemic patient was treated with transfusions and Plethoric one managed with vensections. Literature review was made on this subject.
A Case of Wilson-Mikity Syndrome.
Ra Lee, Young Chul Song, Heung Jae Lee, Keun Soo Lee
Clin Exp Pediatr. 1979;22(9):814-817.   Published online September 15, 1979
A 2 months old male patient with Wilson-Mikity Syndrome was presented. Characteristic clinical manifestations &typical X-ray findings were confirmative for the diagnosis of this syndrome. Pertinent liiteratures &references on Wilson-Mikity syndrome were reviewed briefly.
Case Report
Three Cases of Wilson’s Disease
Hyesook Chang, Heung Jae Lee, Hak Jin Chang, Chong Koo Yun, Sang Hyup Kim
Clin Exp Pediatr. 1975;18(2):145-152.   Published online February 28, 1975
The authors experienced, three cases of Wilson’s disease, which diagnosis were confirmed by family history, their characteristic clinical manifestations with liver and neurological symptoms, Kayser-Fleischer ring and laboratory data with decreased serum ceruloplasmin level and increased 24 hours urine copper excretion. The authors observed their clinical progression after penicillamin therapy. The authors presented these cases and reviewed the referential literatures...
Case Report
Two Cases of Neurofibromatosis
Esook Oh, Soon Young Kim, Heung Jae Lee, Jong Ku Yoon
Clin Exp Pediatr. 1973;16(3):248-252.   Published online March 31, 1973
Presenting two cases of neurofibromatosis, one^with generalized neurofibromatosis and typical family history, and the other with generalized cafe au lait spots and bony defect of the skull which were thought to be early signs of neurofibromatosis, the authors reviewed the referential literatures on the Von Recklinghausen' s disease
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