Scientists dive into the genetics of moebius syndrome
NCT ID NCT02055248
First seen Jun 27, 2026 · Last updated Aug 05, 2026 · Updated 4 times
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.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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Conditions
The condition(s) this trial relates to.
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
Bethesda, Maryland, 20892, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.