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.

  1. 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.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. 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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