Rare genetic Disorder's hidden mental health clues revealed
NCT ID NCT06211673
First seen Oct 31, 2025 · Last updated Jun 18, 2026 · Updated 39 times
Summary
This study looked at 25 people with FOXP1 syndrome, a rare genetic condition that can cause developmental delays and behavioral issues. Researchers used interviews and questionnaires to measure symptoms like hyperactivity, anxiety, and psychosis. The goal was to better understand the mental health challenges in this group, not to test a treatment.
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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.
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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Contacts and locations
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Locations
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Hôpital Necker-Enfants Malades
Paris, 75015, France
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
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