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FOXP1 Post-Puberty Study

January 1, 2022 - January 1, 2023

FOXP1 syndrome is a monogenic condition related to autism. This study will help us to further understand FOXP1 syndrome and its phenotypes. Specifically, it would inform us if there are any specific changes that occur in these adolescents after they go through puberty that are specific to FOXP1 syndrome.

What are the goals of the study?

We are interested in understanding any changes individuals with FOXP1 are experiencing post-puberty, as there have been reports of changes in other neurogenetic disorders.

What will happen during the visit or online?

Parents or caretakers of people with FOXP1 syndrome will complete 3 virtual interviews. Each interview is about 1 to 2 hours. There will also be parent/caretaker questionnaires to complete which would take about an hour.

How will this help families?

This study will help families by identifying more specific phenotypes related to FOXP1 syndrome.

Eligibility Criteria

We are looking to enroll individuals with confirmed FOXP1 syndrome who have gone through puberty and their parents/caretakers.

View the study flyer here.

Contact Information

Hailey Silver – hailey.silver@mssm.edu or Tess Levy – tess.levy@mssm.edu

Research Study Website
Seaver Autism Center for Research and Treatment

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