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Advancing Research 
Empowering Families 

Now Hiring: Executive Director – Click Here for More Information

FOXP1 syndrome is a rare genetic disorder characterized by delays in early motor and language milestones, mild-to-severe intellectual deficits, speech and language impairment and behavior abnormalities.

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INFORMATION AND RESOURCES

Our Mission

The International FOXP1 Foundation is committed to building a global community that empowers and supports families and individuals with FOXP1 syndrome, a rare genetic disorder characterized by delays in early motor and language milestones, mild-to-severe intellectual deficits, speech and language impairment and behavior abnormalities, by sharing knowledge, inspiring hope, encouraging research, and raising awareness.

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Get Involved

Find out how you can contribute to our cause. Whether you want to volunteer your time, donate to our projects, or organize a fundraising event, your support helps us continue our mission.

Join Us

Stay connected with the latest updates from the International FOXP1 Foundation, including global research, fundraising initiatives, and upcoming events in your area.

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Donate

Your donation makes a difference! Every donation helps us continue our mission and support those affected by FOXP1 syndrome. Donations are tax-deductible. 

Citizen Health foxp1
FOXP1 Syndrome Rare genetic disorders Developmental delay disorder Genetic mutations awareness
NORD FOXP1
FOXP1 Syndrome Rare genetic disorders Developmental delay disorder Genetic mutations awareness
Platinum Transparency award
FOXP1 Syndrome Rare genetic disorders Developmental delay disorder Genetic mutations awareness
AGENDA FOXP1
FOXP1 Syndrome Rare genetic disorders Developmental delay disorder Genetic mutations awareness
jumpstart program FOXP1
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