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FOXP1 Syndrome: The Seaver Autism Center for Research and Treatment is Characterizing FOXP1-related Neurodevelopmental Disorders Using Genetic, Medical, and Neuropsychological Measures.
Sponsor: Icahn School of Medicine at Mount Sinai
Summary
FOXP1, also known as Forkhead-box Protein P1, is a transcription factor protein belonging to the FOX gene family. Disruptions in the FOXP1 gene cause a phenotype characterized by global developmental delay, speech deficits, mild dysmorphic features, and traits of autism spectrum disorder. This study seeks to characterize FOXP1-related neurodevelopmental disorders using a number of genetic, medical and neuropsychological measures.
Official title: The Seaver Autism Center for Research and Treatment - Assessment Core
Key Details
Gender
All
Age Range
2 Years - Any
Study Type
OBSERVATIONAL
Enrollment
50
Start Date
2016-03-28
Completion Date
2026-04
Last Updated
2025-04-09
Healthy Volunteers
No
Conditions
Locations (1)
The Seaver Autism Center for Research and Treatment
New York, New York, United States