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Printable card about AS

Provides key facts about Angelman Syndrome, including its genetic cause, symptoms like developmental delays and seizures, and the Foundation’s mission to support families through education and research. It reassures families they are not alone and offers contact details for further resources.

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The mission of 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. We exist to give all of them a reason to smile, with the ultimate goal of finding a cure.

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