Treatment of progressive familial intrahepatic cholestasis: Liver transplantation or partial external biliary diversion
: Progressive intrahepatic familial cholestasis (PFIC), previously called Byler’s disease, is a syndrome in which children develop severe cholestasis progressing to biliary cirrhosis and chronic liver failure, usually during the first decade of life. Clinical features include jaundice, hepatomegaly,...
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Veröffentlicht in: | Pediatric transplantation 1999-08, Vol.3 (3), p.219-224 |
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Sprache: | eng |
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