32 top medical experts on Alpha-Methylacyl-CoA Racemase Deficiency across 7 countries and 2 U.S. states, including 7 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Alpha-Methylacyl-CoA Racemase Deficiency: Congenital bile acid synthesis defect type 4 (BAS defect type 4) is an anomaly of bile acid synthesis (see this term) characterized by mild cholestatic liver disease, fat malabsorption and/or neurological disease.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
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