We are a UK registered charity (1201650) focus on supporting families with Angelman Syndrome, funding research and providing opportunities for physical activity for the Angelman community. Angelman Syndrome (AS) is a rare neurogenetic condition affecting around 1 in 15,000 people, about 500,000 in the world. It affects the nervous system causing severe physical and learning disabilities, little or no speech and issues with movement and balance. A person with Angelman will have near normal life expectancy, but they will require support throughout their life. AS is caused by one of several different types of disruptions of a region of Chromosome 15, all involving a single gene, UBE3A.
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