What is it?
A rare euro-genetic disorder affecting the nervous system, causing developmental delays and intellectual disabilities
Prevalence
Occurs in 1 in 15,000 live births, affecting approximately 500,000 worldwide
Characteristics
Happy Demeanor, developmental delays, speech impairment, and movement and balance problems.
Support
With proper support individuals with AS can live fulfilling lives in their communities.
Helpful Resources
Here are some trusted organizations and resources to learn more about Angelman Syndrome:
Angelman Syndrome Foundation – Research, family support, and awareness.
Cure Angelman Syndrome (FAST) – Focused on funding treatments and potential cures.
National Organization for Rare Disorders (NORD) – Medical information and advocacy.
Genetics Home Reference – MedlinePlus – Detailed medical background.
How You Can Help
Donate – Support foundations funding critical research and family programs
Spread Awareness – Share information to help others understand Angelman Syndrome.
Participate – Join events, walks, and fundraisers to stand with families and individuals impacted by Angelman Syndrome.
