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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.
Angelman syndrome shares symptoms and characteristics with other disorders including autism, cerebral palsy and Prader-Willi syndrome. Due to the common characteristics, misdiagnosis occurs often.
People with Angelman syndrome have developmental problems that become noticeable by the age of 6 – 12 months. Other common signs and symptoms usually appear in early childhood like walking and balance disorders, gastrointestinal issues, seizures and little to no speech. Despite these symptoms, people with Angelman syndrome have an overall happy and excitable demeanor. An individual with AS will light up a room with their smile and laughter.
It is believed that there is a high chance of finding a cure for Angelman syndrome, due to the fact that scientists know what causes AS and have been able to reverse it in mouse models. Find out more about Causes and Types of Angelman syndrome as well as exciting updates on our clinical trials and research towards a cure at www.angelman.org
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. We exist to give all of them a reason to smile, with the ultimate goal of finding a cure.
The Angelman Syndrome Foundation values diversity, equity and inclusion, recognizing the diverse backgrounds and circumstances of those affected by Angelman syndrome. We’re dedicated to creating a culture of respect, equal opportunities, and support for everyone to participate fully in our mission. We believe that diversity enriches our organization, and we’re committed to continuously educating ourselves and others, seeking out diverse perspectives and taking meaningful action to create a more equitable world.
Organization name
Angelman Syndrome Foundation - Sacramento
1992
Mission Category
Health Care
Operating Budget
$1,000,001-$5 million
Organization Need
Funding: Unrestricted
Demographics Served
Individuals with disabilities
BIPOC Leadership
Both the Executive Director & Board Chair
Local Counties Served
Sacramento
Address
3015 E. New York Street A2 #285Sacramento, CA, US
US