Rare genetic Disorder's mental health patterns explored
NCT ID NCT06211673
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study looked at 25 people with FOXP1 syndrome, a rare genetic condition, to better understand their psychiatric symptoms. Researchers used interviews and questionnaires with families to assess hyperactivity, attention, anxiety, autism traits, and more. The goal is to improve recognition and care for mental health issues in this group.
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 lead to better recognition and management of psychiatric symptoms in FOXP1 syndrome.
- What could go wrong
- This is a small, observational study with only 25 participants, so findings may not apply to everyone with FOXP1 syndrome. Some scales used are not yet validated.
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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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Hôpital Necker-Enfants Malades
Paris, 75015, France