J Korean Pediatr Soc.  1977 Feb;20(2):144-147.

A Case of Congenital Biliary Atresia

Affiliations
  • 1Department of Pediatrics, College of Medicine, Korea University, Korea.

Abstract

Congenital biliary atresia is one of rare congenital anomaly of gastrointestinal tract which must be differentiated from neonatal hepatitis. We were experienced congenital biliary atresia was confirmed by surgical exploration, liver biopsy and cholangiography in 2 month-old female infant who was admitted with chief complained of persistent jaundice. Review of literature were also made briefly.


MeSH Terms

Biliary Atresia*
Biopsy
Cholangiography
Female
Gastrointestinal Tract
Hepatitis
Humans
Infant
Jaundice
Liver
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