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Clinical Research Directory

Browse clinical research sites, groups, and studies.

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1 clinical study listed.

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Mental Retardation With Language Impairment and With or Without Autistic Features

Tundra lists 1 Mental Retardation With Language Impairment and With or Without Autistic Features clinical trial. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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RECRUITING

NCT03718923

FOXP1 Syndrome: The Seaver Autism Center for Research and Treatment is Characterizing FOXP1-related Neurodevelopmental Disorders Using Genetic, Medical, and Neuropsychological Measures.

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.

Gender: All

Ages: 2 Years - Any

Updated: 2025-04-09

1 state

FOXP1
Mental Retardation With Language Impairment and With or Without Autistic Features
Autism Spectrum Disorder