Journal of the Korean Pediatric Society 1977;20(2):144-147.
Published online February 28, 1977.
A Case of Congenital Biliary Atresia.
S J Kang, M S Shin, D K Kim, Y C Tockgo
Department of Pediatrics, College of Medicine, Korea University, Korea.
先天性 膽管發育 不全症 1例
강세진, 신명식, 김덕경, 독고영창
고려대학교 의과대학 소아과학교실
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.




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