259 top medical experts on Hyperlipoproteinemia Type I across 40 countries and 21 U.S. states, including 105 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Hyperlipoproteinemia Type I: An inherited condition due to a deficiency of either lipoprotein lipase or apolipoprotein C-II (a lipase-activating protein). The lack of lipase activities results in inability to remove chylomicrons and triglycerides from the blood which has a creamy top layer after standing.
  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), Hyperlipoproteinemias (515).
  4. Clinical Trials ClinicalTrials.gov : at least 24 including 3 Active, 10 Completed, 5 Recruiting
  5. Synonyms: Apolipoprotein C-II Deficiency,  Familial Hyperchylomicronemia,  Familial Lipoprotein Lipase Deficiency


  

        

                    


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