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Facts About Angelman Syndrome

Angelman Syndrome Foundation, Inc.
Provided here with the express permission of Angelman Syndrome Foundation, Inc. as originally published on their website.
Facts about AS was initially a small booklet developed in 1987 to help launch the Angelman Syndrome Foundation organization and to help inform parents and professionals about the syndrome. The Facts document is now in its seventh edition. Over the years, it has grown in scope and complexity and this year the “pamphlet/brochure” has been reformatted for a web presence.
Get the Angelman Sydrome Facts Booklet HERE
Featured Organization: Angelman Syndrome Foundation, Inc.
The Angelman Syndrome Foundation’s mission is to advance the awareness and treatment of Angelman Syndrome througheducation and information, research, and support for individuals with Angelman Syndrome, their families and other concerned parties.
ASF is a national 501©(3) organization dedicated to helping families, care providers and medical professionals arm themselves with as much helpful information about Angelman Syndrome as possible. The ASF sponsors a biennial conference which gives you the opportunity to hear the latest research results, therapeutic techniques, educational strategies, long-term planning and financial planning information. The conference also offers many networking opportunities to talk to familiies that are dealing with the same issues you might be having while caring for an individual with Angelman Syndrome.
Please support our contributing organization and visit Angelman Syndrome Foundation, Inc.

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