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Creating a Future with Endless Possibilities

FOXP1 Syndrome is registered with  

the Europe PMC


What is the Europe PMC?

It is a global, free database of life science publications.   

PMC provides openly available peer-reviewed scientific research.

How can this help us support your fox child?

Share the link with all your clinical practitioners to help them better understand and treat your child with FOXP1 syndrome.​

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Our mission is to build a global community that empowers and supports families and individuals with FOXP1 syndrome by sharing knowledge, inspiring hope, encouraging research, and raising awareness.



"While there is still so much unknown and no real changes in our day-to-day life with the diagnosis, it was a relief to have an answer and explanation for everything about Joey that had felt "off". It is amazing to feel the support from the other families and to know we are not alone."

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