Dr. Robert Carson delves into his studies on movement disorders, particularly myoclonus, in individuals with Angelman syndrome. He emphasizes the importance of characterizing these abnormal movements to develop effective treatments. The research involves analyzing video data submitted by caregivers, which is then reviewed by a panel of specialists to classify and better understand the movements. This collaborative approach aims to standardize terminology and guide future therapeutic strategies.
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.