Scientists hunt for eye disease genes in 2,000-Person study

NCT ID NCT02077894

First seen Jun 27, 2026 · Last updated Jun 27, 2026

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.

Disclaimer Read more

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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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • National Institutes of Health Clinical Center,

    RECRUITING

    Bethesda, Maryland, 20892, United States

    Contact Phone: •••-•••-•••• Email: •••••@•••••