87 top medical experts on Apolipoprotein B Familial Hypobetalipoproteinemia across 9 countries and 5 U.S. states, including 13 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Apolipoprotein B Familial Hypobetalipoproteinemia: An autosomal dominant disorder of lipid metabolism. It is caused by mutations of apolipoproteins B, main components of chylomicrons and beta-lipoproteins (low density lipoproteins or LDL). Features include abnormally low LDL, normal triglyceride level, and dietary fat malabsorption.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Inborn Errors Lipid Metabolism (797), Hypobetalipoproteinemias (370).
  4. Clinical Trials ClinicalTrials.gov : at least 1 including 1 Completed
  5. Synonyms: Apolipoprotein B Deficiency


  

        

                    


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