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A case of Finnish Type of Congenital Nephrotic Syndrome.

Journal of the Korean Pediatric Society 1982;25(2):175-182.
Published online February 28, 1982.
A case of Finnish Type of Congenital Nephrotic Syndrome.
Jeong Sik Min1, Yang Kook Shon1, Soo Woong Lee1, Suk Chul Kang1, Yong Koo Park2, Moon Ho Yang2
1Department of Pediatrics, College of Medicine, Kyung Hee University, Seoul, Korea.
2Department of Pathology, College of Medicine, Kyung Hee University, Seoul, Korea.
선천성 신증후군, 휘니쉬형 1 례
민정식1, 손양국1, 이수웅1, 강석철1, 박용구2, 양문호2
1경희대학교 의과대학 소아과학교실
2경희대학교 의과대학 병리학교실
Abstract
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 died of pneumonia at 5 1/2 months of age. The diagnosis was made by birth history, clinical manifestation, laboratory findings and finally by the autopsy findings, Literatures are reviewed briefly.
Key Words: Nephrotic Syndrome, Congenital, Finnish type


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