Progressive familial intrahepatic cholestasis type 2 (Q54492): Difference between revisions
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A colestase intra-hepática familiar progressiva tipo 2 (PFIC2), um tipo de colestase intra-hepática familiar progressiva , é uma patologia hereditária neonatal grave da formação de bílis. Trata-se de uma colestase de origem hepatocelular e não associada a características extra-hepáticas. Inicialmente, a PFIC2 foi descrita com o nome de síndrome de Byler.. | |||
| description / en | description / en | ||
Progressive familial intrahepatic cholestasis type 2 (PFIC2), a type of progressive familial intrahepatic cholestasis (PFIC), is a severe, neonatal, hereditary disorder in bile formation that is hepatocellular in origin and not associated with extrahepatic features. Initially, PFIC2 was reported under the name Byler syndrome. | |||
Revision as of 02:07, 14 August 2026
Progressive familial intrahepatic cholestasis type 2 (PFIC2), a type of progressive familial intrahepatic cholestasis (PFIC), is a severe, neonatal, hereditary disorder in bile formation that is hepatocellular in origin and not associated with extrahepatic features. Initially, PFIC2 was reported under the name Byler syndrome.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1168921980 |
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| English | Progressive familial intrahepatic cholestasis type 2 |
Progressive familial intrahepatic cholestasis type 2 (PFIC2), a type of progressive familial intrahepatic cholestasis (PFIC), is a severe, neonatal, hereditary disorder in bile formation that is hepatocellular in origin and not associated with extrahepatic features. Initially, PFIC2 was reported under the name Byler syndrome. |
