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Livers transplantation for children suffering from congenital biliary atresia in the National Institute of Pediatrics
Article in Vi | WPRIM | ID: wpr-1697
Responsible library: WPRO
ABSTRACT
During 5 years (1994-1998), 147 children suffering from congenital biliary atresia were admitted to NIP. Clinical manifestations include icterus, discolored stool and hepatomegaly. The gallbladder is absent; ultrasonography shows that its diameter doesn't change before, during and after meal in all patients. 136 patients among those children require a liver's transplantation. It means that, every years, there were 27 children suffering from biliary atresia who require a liver's transplantation.
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Full text: 1 Index: WPRIM Main subject: Biliary Atresia / Liver Transplantation Language: Vi Journal: Journal of Medical and Pharmaceutical Information Year: 2001 Type: Article
Full text: 1 Index: WPRIM Main subject: Biliary Atresia / Liver Transplantation Language: Vi Journal: Journal of Medical and Pharmaceutical Information Year: 2001 Type: Article