Scientists hunt for hidden genes behind inherited eye conditions
NCT ID NCT02077894
First seen Sep 30, 2025 · Last updated May 14, 2026 · Updated 24 times
Summary
This study aims to identify the genetic causes of inherited eye diseases by analyzing the DNA of up to 2,000 participants, including affected individuals and their family members. Researchers will use whole exome or whole genome sequencing to find new or known gene mutations. The goal is to improve understanding and diagnosis of these conditions, not to provide a treatment or cure.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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National Institutes of Health Clinical Center,
RECRUITINGBethesda, Maryland, 20892, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
Explore the condition pages connected to this study.