Scientists hunt for Eye-Misalignment genes

NCT ID NCT04770519

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study aims to find genetic variants linked to strabismus (crossed eyes) and nystagmus (involuntary eye movements). Researchers will analyze DNA from families with at least three members who have strabismus, or families with infantile esotropia or nystagmus. By comparing affected and unaffected relatives, they hope to identify shared genetic changes. The study is observational and does not test any 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 study could identify genes that cause strabismus and nystagmus, pointing toward future genetic tests or therapies.

What could go wrong

This is an observational study, not a treatment trial. Finding genetic links does not guarantee new treatments, and results may take years to apply.

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.

congenital nystagmus esotropia exotropia pathologic nystagmus strabismus

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

  • Boston Children's Hospital

    RECRUITING

    Boston, Massachusetts, 02115, United States

    Contact Email: •••••@•••••