531 top medical experts on Fabry Disease across 46 countries and 31 U.S. states, including 398 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Fabry Disease: An X-linked inherited metabolic disease caused by a deficiency of lysosomal alpha-galactosidase A. It is characterized by intralysosomal accumulation of globotriaosylceramide and other glycosphingolipids in blood vessels throughout the body leading to multi-system complications including renal, cardiac, cerebrovascular, and skin disorders.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): X-Linked Genetic Diseases (2,304), Sphingolipidoses (136), Cerebral Small Vessel Diseases (1,480).
  4. Clinical Trials ClinicalTrials.gov : at least 187 including 10 Active, 86 Completed, 30 Recruiting
  5. Synonyms: Anderson-Fabry Disease,  Angiokeratoma Corporis Diffusum


  

        

                    


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