242 top medical experts on progressive familial intrahepatic 1 Cholestasis across 38 countries and 17 U.S. states, including 89 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. progressive familial intrahepatic 1 Cholestasis: PFIC1, a type of progressive familial intrahepathic cholestasis (PFIC, see this term), is an infantile hereditary disorder in bile formation that is hepatocellular in origin and associated with extrahepatic features.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Byler disease,  Byler's disease,  1 Benign Recurrent Intrahepatic Cholestasis,  1 Progressive Familial Intrahepatic Cholestasis,  benign recurrent intrahepatic 1 Cholestasis,  fatal intrahepatic Cholestasis,  FIC1 deficiency,  PFIC1 Progressive familial intrahepatic cholestasis type 1,  Progressive familial intrahepatic cholestasis,  Progressive familial intrahepatic cholestasis type 1 (PFIC 1),  Progressive familial intrahepatic cholestasis type 1 (PFIC1),  Summerskill syndrome


  

        

                    


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