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A case of Finnish Type of Congenital Nephrotic Syndrome
Journal of the Korean Pediatric Society ; : 175-182, 1982.
Article in Korean | WPRIM | ID: wpr-214475
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.
Subject(s)

Full text: Available Index: WPRIM (Western Pacific) Main subject: Placenta / Pneumonia / Autopsy / Reproductive History / Growth and Development / Diagnosis / Edema / Nephrotic Syndrome Type of study: Diagnostic study Limits: Female / Humans Language: Korean Journal: Journal of the Korean Pediatric Society Year: 1982 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Placenta / Pneumonia / Autopsy / Reproductive History / Growth and Development / Diagnosis / Edema / Nephrotic Syndrome Type of study: Diagnostic study Limits: Female / Humans Language: Korean Journal: Journal of the Korean Pediatric Society Year: 1982 Type: Article