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The ASF is a nonprofit organization that helps families and individuals with Angelman syndrome live better lives. It funds research, provides clinical care, offers educational resources and hosts fundraisers and events.
- What is Angelman Syndrome
Angelman syndrome (AS) is a rare neuro-genetic disorder that...
- For Parents
For Parents - Angelman Syndrome Foundation – With you for...
- Make an Impact
The Angelman Syndrome Foundation has funded life-changing...
- Events
Events - Angelman Syndrome Foundation – With you for the...
- About
About - Angelman Syndrome Foundation – With you for the...
- Symptoms and Causes
Symptoms and Causes - Angelman Syndrome Foundation – With...
- Testing and Diagnosis
Testing and Diagnosis - Angelman Syndrome Foundation – With...
- Genetics of AS
Genetics of AS - Angelman Syndrome Foundation – With you for...
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Photo Gallery - Angelman Syndrome Foundation – With you for...
- What is Angelman Syndrome
Angelman syndrome (AS) is a rare neuro-genetic disorder that occurs in one in 15,000 live births or 500,000 people worldwide. It is caused by a loss of function of the UBE3A gene in the 15th chromosome derived from the mother.
Learn about the Angelman Syndrome Foundation, a non-profit organization that aims to advance awareness, treatment, and support for individuals with Angelman syndrome and their families. Meet our staff, board, and learn about our strategic plan, diversity, equity and inclusion, and AS clinics.
Angelman Syndrome Foundation, Aurora, Illinois. 26,607 likes · 374 talking about this · 275 were here. The Angelman Syndrome Foundation works to advance the awareness and treatment of Angelman Syndrome t
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ASF is a non-profit organization that promotes awareness, research, and support for Angelman syndrome, a rare genetic disorder. Learn about the symptoms, diagnosis, treatment, and prevention of this condition from ASF and other sources.
FAST is the leading patient advocacy organization working to cure Angelman syndrome. As the largest non-governmental funder of Angelman syndrome research in the world, our goal is to drive forward transformative research and development programs as quickly as possible for those living with Angelman syndrome—regardless of age or genotype.
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FAST is the leading patient advocacy organization working to cure Angelman syndrome. As the largest non-governmental funder of Angelman syndrome research in the world, our goal is to drive forward transformative research and development programs as quickly as possible for those living with Angelman syndrome—regardless of age or genotype.