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Community

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

News & Events

Inaugural FBXO31 Foundation Family Roundtable

April 11, 2024

Washington University, St. Louis
To register & for more information
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International Registry

We are building a direct to patient International Registry to gather much needed patient information to guide our ongoing research and future drug trials. Please register your patient today – all information is completely confidential

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FBXO31 Stories

We’re collecting stories about patients and families affected by FBXO31. If you are interested in sharing your journey, we would love to hear from you.

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How to Help

Contribute to shaping a brighter tomorrow for those impacted by a FBXO31 disorder.

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Are you, or someone you know, affected by FBXO31-related cerebral palsy?

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The content provided by this website is for educational, communication and information purposes only and is not intended to replace or constitute medical advice or treatments. Consult your own physician.

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