$103,000
As individuals with Angelman syndrome get older, there is often an increase in the frequency of abnormal movements, including nonepileptic myoclonus. The goal of this study is to better characterize these abnormal movements to help us identify new ways of treating patients with them.
This study will use video data provided by Angelman families on the front end and a large team of movement disorders specialists who will evaluate the videos on the tail end. The study was designed to be family friendly, making it easy to be a part of.
Watch Dr. Carson discuss the project with Terry Jo Bichell
Results
Published paper on Gelastic Spells
See the family-friendly report
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.