Scientists map genes behind rare childhood vision loss
NCT ID NCT00055029
Summary
This study aims to understand the causes and progression of X-linked juvenile retinoschisis (XLRS), a rare inherited eye disease that causes worsening vision loss in boys and young men. Researchers are enrolling affected males and their family members to examine their eyes, take pictures of the retina, and analyze blood samples for genetic clues. The goal is to connect specific genetic changes with the severity of eye problems to help guide future treatment research.
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Contacts and locations
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Locations
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National Institutes of Health Clinical Center
Bethesda, Maryland, 20892, United States
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William Beaumont Hospital
Rochester, Michigan, 48309, United States
Conditions
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