553 top medical experts on Retinitis Pigmentosa across 40 countries and 32 U.S. states, including 488 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Retinitis Pigmentosa: Hereditary, progressive degeneration of the retina due to death of ROD photoreceptors initially and subsequent death of cone photoreceptors. It is characterized by deposition of pigment in the retina.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Hereditary Eye Diseases (476) and Narrower Categories: Alstrom Syndrome (273), Bardet-Biedl Syndrome (681), Kearns-Sayre Syndrome (267), Usher Syndromes (725).
  4. Clinical Trials ClinicalTrials.gov : at least 139 including 8 Active, 59 Completed, 39 Recruiting
  5. Synonyms: Pigmentary Retinopathy, Tapetoretinal Degeneration




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