Fraxa Research Foundation, Inc.
FRAXA's mission is to find effective treatments and ultimately a cure for Fragile X syndrome and are likely to help people affected by autism. Our mission is to find a effective treatments and ultimately a cure for fragile X syndrome, the most common inherited cause of autism. We directly fund research grants and fellowships at top universities around the world. FRAXA was founded in 1994 by three parents of children with fragile X. Fragile X Syndrome is the most common inherited cause of autism and intellectual disabilities. It affects 1 in 4000 boys and 1 in 6000 girls worldwide, and one in 260 women and 1 in 800 men are carriers. Treatments for fragile X are likely to help people affected by related disorders including autism, Alzheimers, and many other brain disorders.
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1994
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Fragile X Syndrome Research & Treatment • FRAXA Research Foundation - Finding a Cure for Fragile X FRAXA Research Foundation Finding a Cure for Fragile X Syndrome Accelerating Fragile X Research for Effective Treatments Discovering Effective Treatments A Cure for Fragile X Syndrome Your support enables FRAXA Research Foundation to fund groundbreaking research and lifechanging clinical trials. How Does FRAXA Help. FRAXAs mission is to find effective treatments and ultimately a cure for Fragile X syndrome. We directly fund research grants and fellowships at top universities around the world.
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