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Case Report
Two Cases of Acute Form of Tyrosinemia Type I
Kyu Tae Kim, Young Mi Kim, Su Eun Park, Sang Ook Nam, Jae Hong Park
Clin Exp Pediatr. 2002;45(1):131-136.   Published online January 15, 2002
Tyrosinemia type I is an autosomal recessive disorder of amino acid metabolism and is caused by a deficiency of fumarylacetoacetate hydrolase(FAH), the last enzyme in the catabolic pathway of tyrosine. The disease is characterized by hepatic dysfunction, hepatocellular carcinomas, renal tubular dysfunction, rickets, and neurologic crises. We experienced 2 cases(a 4-day-old girl, a 7- month-old girl) of acute form of tyrosinemia type I. Case...
Original Article
A Study on Coagulopathy in High-risk Neonates.
Chae Sup Yoo, H. W. Lee, Keun Lee, Moon Ja Kim
Clin Exp Pediatr. 1988;31(11):1445-1452.   Published online November 30, 1988
Life threatening neonatal hemorrhage is a common problem in Nursery Intensive Care Unit. It is associated with asphyxia, intracranial hemorrhage, and hyaline membrane disease, and develops to D.I.C., which attributes to neonatal mortality and morbidity. Clinical study was performed on 32 high-risk neonates and 20 mild illness cases, who had been admitted to Department of Pediatrics, Ewha University Hospital, during the period of 2.6...
Case Report
A Case of Kasabach-Merritt Syndrome.
Young Yoon choi, young Hwa park, Hyung Suk byun, Chull sohn, Ae Sook kim
Clin Exp Pediatr. 1982;25(3):310-316.   Published online March 31, 1982
Hemangioma associated with thrombocytopenia is a relatively rare occurrence. The first case was described in 1940 by Kasabach and Merritt, who used X-ray therapy as radium implants in the treatment of hemangioma on the affected infant. The tumor regressed and the platelet count rose to normal. Mechanical sequestration of platelets in the vascular channels of the hemangioma is believed to be the mechanism of...
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