216 top medical experts on Stargardt Disease across 24 countries and 14 U.S. states, including 47 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Stargardt Disease: A juvenile-onset macular dystrophy characterized by progressive loss of visual acuity with normal acuity in peripheral visual fields. Other associated clinical features may include lipofuscin fundus autofluorescence, atrophy of the retinal pigment epithelium, loss of color vision, photophobia and paracentral scotoma. Germline mutations in the abca4 gene have been identified in recessive and dominant diseases.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Broader Categories (#Experts): Hereditary Eye Diseases (901).
- Clinical Trials : at least 39 including 3 Active, 19 Completed, 9 Recruiting
- Synonyms: Juvenile Macular Degeneration, Stargardt Disease 1
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