215 top medical experts on Familial Partial Lipodystrophy across 26 countries and 9 U.S. states, including 48 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Familial Partial Lipodystrophy: Inherited conditions characterized by the partial loss of adipose tissue, either confined to the extremities with normal or increased fat deposits on the face, neck and trunk (type 1), or confined to the loss of subcutaneous FAT from the limbs and trunk (type 2). Type 3 is associated with mutation in the gene encoding peroxisome proliferator-activated receptor gamma.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Lipodystrophy (3,179), Inborn Errors Lipid Metabolism (797), Laminopathies (306).
  4. Clinical Trials ClinicalTrials.gov : at least 12 including 1 Active, 4 Completed, 3 Recruiting


  

        

                    


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