Angelman Syndrome

Vanderbilt University Medical Center and the Angelman Syndrome Foundation announced March 23 the official opening of the Angelman Syndrome Clinic at Vanderbilt, one of only five Angelman syndrome-specific clinics in the country. Read More

A mutation associated with epilepsy and autism also is responsible for a “pale eye” trait in two rare genetic disorders, Angelman syndrome and Prader-Willi syndrome, neuroscientists at Vanderbilt University Medical Center reported this week. Read More

It’s a story of love and determination and a debilitating lifelong disorder. A son’s rare genetic disease has led his mom to become a scientist at Vanderbilt University. Watch this VUCast Extra and a mom’s race against time. Read More

Vanderbilt biologists have found a direct link between the biological clock and Angelman syndrome, a neurogenetic disorder that occurs in more than one in every 15,000 live births. The link may provide a valuable way to judge the effectiveness of the first experimental drugs under development for treating the syndrome. Read More