Scientists hunt for eye disease genes in 2,000-Person study
NCT ID NCT02077894
First seen Jun 27, 2026 · Last updated Jul 29, 2026 · Updated 8 times
Summary
This study aims to find the genetic causes of inherited eye conditions by analyzing the DNA of 2,000 people, including affected individuals and their family members. Researchers will use whole exome or whole genome sequencing to look for new or known gene mutations. The goal is to improve understanding and diagnosis of these eye diseases.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- What this could lead to
- If successful, this study could identify new genes linked to inherited eye diseases, leading to better genetic testing and diagnosis for patients and families.
- What could go wrong
- This is an observational study, not a treatment trial. It may not directly benefit participants, and finding a genetic cause is not guaranteed for everyone.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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National Institutes of Health Clinical Center,
RECRUITINGBethesda, Maryland, 20892, United States
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