26 top medical experts on 1 congenital Bile acid synthesis defect across 4 countries, including 3 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. 1 congenital Bile acid synthesis defect: Congenital bile acid synthesis defect type 1 (BAS defect type 1) is the most common anomaly of bile acid synthesis (see this term) characterized by variable manifestations of progressive cholestatic liver disease, and fat malabsorption.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: Deficiency Of 3-Beta-Hydroxy-Delta-5-C27-Steroid Oxidoreductase,  3-beta-hydroxy-delta-5-C27-steroid oxidoreductase deficiency,  progressive familial intrahepatic 4 Cholestasis,  Congenital Bile Acid Synthesis Defect Type 1 (CBAS1),  PFIC4 Progressive familial intrahepatic cholestasis type 4,  Progressive familial intrahepatic cholestasis 4


  

        

                    


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