Terry Jo Bichell and Dr. Robert Carson discuss recent developments in Angelman syndrome research, focusing on Dr. Carson’s new study on myoclonus. They explore the implications of this research for understanding and managing Angelman syndrome, providing valuable insights for families and caregivers.
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.