The FOUND Study - FOXP1 Syndrome: Understanding Through Neruodevelopmental Deep Phenotyping to Support Clinical Trials
PI: Rujuta Wilson, MD
Eligibility:
Your family may be eligible for this study if you or your child has a diagnosis of FOXP1 Syndrome and:
- Is between 1 to 20 years old
- Live anywhere in North America
Purpose:
- Behavioral/cognitive assessments
- Neurological/physical exam
- Gait/Upper extremity assessments
- Parent interview/questionnaire
Benefits:
You will receive:
- $50 gift card upon baseline completion
- Clinical feedback
Contact:
found-study@mednet.ucla.edu
