204 top medical experts on progressive familial intrahepatic 3 Cholestasis across 25 countries and 9 U.S. states, including 30 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- progressive familial intrahepatic 3 Cholestasis: Progressive familial intrahepatic cholestasis type 3 (PFIC3), a type of progressive familial intrahepatic cholestasis (PFIC, see this term), is a late-onset hereditary disorder in bile formation that is hepatocellular in origin. Onset may occur from infancy to young adulthood.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Synonyms: Abcb4-Related Intrahepatic Cholestasis, 3 Progressive Familial Intrahepatic Cholestasis, with Elevated Serum Gamma-Glutamyltransferase Progressive Familial Intrahepatic Cholestasis, Low gamma-GT Familial Intrahepatic Cholestasis, MDR3 Deficiency, PFIC3 Progressive familial intrahepatic cholestasis type 3, Progressive Familial Intrahepatic Cholestasis 3 (PFIC 3), Progressive Familial Intrahepatic Cholestasis 3 (PFIC3), Progressive familial intrahepatic cholestasis with elevated serum gamma-glutamyltransferase
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