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.
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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