Site © 2017-2019 by CTNNB1 Syndrome Awareness Worldwide (CSAW).  The information contained in this site should not be construed as a substitute for personal medical advice. Please consult with a qualified clinician in all matters relating to genetic diagnosis, management and health. 

 

CSAW Family and Friends,

Yesterday saw the launch of our sister organization, ACCT (Advancing CTNNB1 Cures and Treatments)...more

the official website of  CTNNB1 Syndrome Awareness Worldwide (CSAW)

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What is CTNNB1 Syndrome?

CTNNB1 Syndrome refers to complications resulting from either a mutation or deletion of the CTNNB1 gene. Depending on the degree of alteration or mutation (and the alteration of other genes), there will be a wide range of abilities that are affected in subjects with CTNNB1 Syndrome.  Currently, there are just over 150 people in the world known to be diagnosed with CTNNB1 Syndrome.  See 'SYNDROME INFO.' for a more detailed description of CTNNB1 Syndrome.

Our mission is to create awareness of CTNNB1 Syndrome; provide information about symptoms, diagnosis, treatments and therapies; and connect affected families.

There are many ways, beyond financial support, for you to help us get the word out about CTNNB1 Syndrome.  Check out how you can help!

Your donation, no matter how small it may seem to you, will go a long way to support our mission!