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.
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.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for FOXP1 SYNDROME are added.
Genom att skicka in godkänner du våra Användarvillkor
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
Genom att skicka in godkänner du våra Användarvillkor
Locations
-
Hôpital Necker-Enfants Malades
Paris, 75015, France
Conditions
Explore the condition pages connected to this study.