CTNNB1 Syndrome Network

CTNNB1 Syndrome Network is designed to support families navigating CTNNB1 Syndrome, a rare genetic disease.

It shares community news and educational resources. You can check the latest events for the community and add them to your calendar.

Check the latest news in research coming from our parents non-profit organizations. Get notifications when something important comes up.

Ask our chatbot about CTNNB1 Syndrome, and about relevant information coming from parents organizations.

CTNNB1 Syndrome Network does not provide medical advice, diagnosis, or treatment. Consult qualified healthcare professionals for medical guidance.

CTNNB1 app available now in English, Spanish, French, Italian, Portuguese, German, Polish & Slovenian. Get resources and news in your language today.

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