A new peer-reviewed study has officially named our condition — Kruer syndrome — and published the most complete clinical picture of FBXO31 p.Asp334Asn to date.

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FBXO31 Genetic Mutation Linked to Cerebral Palsy

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The FBXO31 Foundation has been formed to Connect and Support patients and Fund Research for a cure.

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The FBXO31 Foundation fosters opportunities for patients and families affected by FBXO31 to connect and share their stories.

Science

Our foundation funds cutting edge research to benefit those with FBXO31.

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