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FOXG1 Research Foundation
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Support FOXG1 Fundraising Teams
Support FOXG1 Fundraising Teams
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November is FOXG1 syndrome awareness month, and we’re sharing these incredible children with a daily dose of laughter - we dare you not to smile! FOXG1 syndrome is a rare, neurological disorder that impacts brain development and typically causes epilepsy, as well as a spectrum of severe to moderate physical and cognitive disabilities. Mutations to the FOXG1 gene are mostly (de-novo) non-inherited. There are currently more than 700 known people in the world diagnosed with FOXG1 syndrome. #DailyDo
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