Dr. Robert Carson discusses his research on movement disorders and myoclonus in individuals with Angelman syndrome. He explores the underlying causes of these motor challenges, their impact on daily life, and potential treatment approaches. The presentation provides valuable insights for caregivers, families, and healthcare professionals seeking to better understand and manage movement-related symptoms in Angelman syndrome.
The mission of 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.