450 top medical experts on Hereditary Eye Diseases across 32 countries and 25 U.S. states, including 366 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Hereditary Eye Diseases: Transmission of gene defects or chromosomal aberrations/abnormalities which are expressed in extreme variation in the structure or function of the eye. These may be evident at birth, but may be manifested later with progression of the disorder.
  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 Genetic Diseases (2,477) and Narrower Categories: Aicardi Syndrome (452), Albinism (840), Aniridia (1,153), Choroideremia (693), Coloboma (1,958), Cone-Rod Dystrophies (783), Duane Retraction Syndrome (611), Familial Exudative Vitreoretinopathies (211), Graves Ophthalmopathy (1,451), Gyrate Atrophy (251), Hereditary Corneal Dystrophies (949), Hereditary Optic Atrophies (523), Optic Nerve Hypoplasia (137), Retinal Dysplasia (235), Retinitis Pigmentosa (2,594), Retinoblastoma (2,111), Stargardt Disease (515), Vitelliform Macular Dystrophy (898), Walker-Warburg Syndrome (732), Weill-Marchesani Syndrome (187).
  4. Clinical Trials ClinicalTrials.gov : at least 21 including 6 Active, 7 Completed, 6 Recruiting


  

        

                    


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