225 top medical experts on Niemann-Pick Diseases across 25 countries and 18 U.S. states, including 62 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Niemann-Pick Diseases: A group of autosomal recessive disorders in which harmful quantities of lipids accumulate in the viscera and the central nervous system. They can be caused by deficiencies of enzyme activities (sphingomyelin phosphodiesterase) or defects in intracellular transport, resulting in the accumulation of sphingomyelins and cholesterol. There are various subtypes based on their clinical and genetic differences.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Non-Langerhans-Cell Histiocytosis (893), Sphingolipidoses (136) and Narrower Categories: Type A Niemann-Pick Disease (350), Type B Niemann-Pick Disease (336), Type C Niemann-Pick Disease (862).
  4. Clinical Trials ClinicalTrials.gov : at least 50 including 11 Active, 20 Completed, 6 Recruiting
  5. Synonyms: Niemann-Pick Disease


  

        

                    


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