J Korean Pediatr Soc.  1982 Feb;25(2):175-182.

A case of Finnish Type of Congenital Nephrotic Syndrome

Affiliations
  • 1Department of Pediatrics, College of Medicine, Kyung Hee University, Seoul, Korea.
  • 2Department of Pathology, College of Medicine, Kyung Hee University, Seoul, Korea.

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.

Keyword

Nephrotic Syndrome; Congenital; Finnish type

MeSH Terms

Autopsy
Diagnosis
Edema
Female
Growth and Development
Humans
Nephrotic Syndrome*
Placenta
Pneumonia
Reproductive History
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