Scientists dive into the genetics of moebius syndrome

NCT ID NCT02055248

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

Summary

This completed study by the National Human Genome Research Institute looked at 207 people with Moebius syndrome or similar congenital facial weakness disorders, along with their family members. Researchers aimed to better understand the genetic and clinical features of these conditions through detailed evaluations over 3-5 days. The study did not test any treatment but focused on gathering information to help future research.

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 improve understanding of the genetic causes of Moebius syndrome, potentially pointing toward future diagnostic or therapeutic approaches.

What could go wrong

This is an observational study, not a treatment trial. It aims to gather knowledge, not test a cure or therapy, so direct patient benefits are not expected.

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.

brain disorder Congenital Abnormalities Mobius syndrome

As listed by the trial registrant

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

Contacts and locations

Locations

  • National Institutes of Health Clinical Center

    Bethesda, Maryland, 20892, United States