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
Hauptverfasser: Ismail, Hor, Kaliciński, Piotr, Markiewicz, Małgorzata, Jankowska, Irena, Pawłowska, Joanna, Kluge, Przemysław, Eliadou, Eliana, Kamiński, Andrzej, Szymczak, Marek, Drewniak, Tomasz, Revillon, Yann
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Sprache:eng
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