Scientists hunt for genes behind worst cases of rare eye condition

NCT ID NCT02886611

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

Summary

This study is looking at 60 people with a genetic eye surface disease called limbal stem cell deficiency. Researchers want to find out if certain gene changes are linked to more severe disease. They will compare patients' genes with their eye health to look for patterns. This is an observational study, so it does not test any new treatment.

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 could help doctors predict which patients with genetic eye surface disease will have the most severe symptoms, guiding earlier and more personalized care.

What could go wrong

This is an observational study, not a treatment trial. It will not directly improve any patient's condition, and the genetic links found may not lead to new therapies.

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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Conditions

The condition(s) this trial relates to.

limbal stem cell deficiency

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: •••••@•••••

Locations

  • Fondation Ophtalmologique Adolphe de Rothschild

    RECRUITING

    Paris, 75019, France

    Contact