385 top medical experts on Inborn Errors Lipid Metabolism across 35 countries and 26 U.S. states, including 259 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Inborn Errors Lipid Metabolism: Errors in the metabolism of lipids resulting from inborn genetic mutations that are heritable.
  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 Metabolism (1,547), Lipid Metabolism Disorders (1,364) and Narrower Categories: Apolipoprotein B Familial Hypobetalipoproteinemia (87), Barth Syndrome (690), Cerebrotendinous Xanthomatosis (762), Congenital Generalized Lipodystrophy (851), Familial Combined Hyperlipidemia (496), Familial Partial Lipodystrophy (565), Hyperlipoproteinemia Type I (753), Hyperlipoproteinemia Type II (2,231), Hyperlipoproteinemia Type III (190), Hyperlipoproteinemia Type IV (140), Hyperlipoproteinemia Type V (73), Hypolipoproteinemias (202), Lipidoses (578), Shwachman-Diamond Syndrome (330), Smith-Lemli-Opitz Syndrome (603).
  4. Clinical Trials ClinicalTrials.gov : at least 25 including 1 Active, 13 Completed, 1 Recruiting


  

        

                    


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