Rare genetic disorder linked to complex mental health challenges
NCT ID NCT06211673
Summary
This study aimed to better understand the psychiatric symptoms experienced by people with FOXP1 syndrome, a rare genetic disorder. Researchers observed 25 participants to document conditions like ADHD, autism, anxiety, and psychosis that often accompany the syndrome. The goal was to improve future care by identifying patterns and testing assessment tools specifically for this population.
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Contacts and locations
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Locations
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Hôpital Necker-Enfants Malades
Paris, 75015, France
Conditions
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