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

Locations

  • National Institutes of Health Clinical Center

    Bethesda, Maryland, 20892, United States

  • William Beaumont Hospital

    Rochester, Michigan, 48309, United States

Conditions

Explore the condition pages connected to this study.