The Mission of the Angelman Syndrome Foundation is to advance the awareness and treatment of Angelman Syndrome through education and information, research, and support for individuals with Angelman Syndrome, their families, and other concerned parties.
Angelman Syndrome has confounded and confused the medical community and parents of Angelman individuals for hundreds of years. Initially presumed to be rare, it is now believed thousands of Angelman Syndrome cases have gone undiagnosed or misdiagnosed as cerebral palsy, autism or other childhood disorders. Our vision is to improve the lives of individuals with AS and their families. We hope you will join us!
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