Angelman syndrome is a genetic condition that affects the nervous system. It usually isn’t detected until developmental delays become noticeable, such as speech and balance, mental disability, and seizures.
Delays in maturing, called developmental delays, begin between about 6-12 months of age. The delays often are the first signs of Angelman syndrome. Seizures may begin between the ages of 2-3 years old.
People with Angelman syndrome tend to live close to a typical life span. But the condition can’t be cured. Treatment focuses on managing medical, sleep and developmental issues.
Bright Expectations
Find information on evaluation and intervention services, support programs for families, resources for health care providers, and information on developmental disabilities
Resources
Angelman Syndrome Foundation advances the awareness and treatment of Angelman syndrome through education and information, research, and support for individuals with Angelman syndrome, their families, and friends.Â
Foundation for Angelman Syndrome Therapeutics is run by an all-volunteer board parents and professionals dedicated to finding a cure for AS and related conditions.