“My team is so grateful for this designation and for the support from the Angelman Syndrome Foundation,” said Diana Walleigh, MD, epileptologist and Director of the Chromosome 15 and Related Disorders Clinic. “Our patients and families are amazing – there’s so much potential in each of our patients... With this new designation we are hopeful to work toward finding a potential cure for AS, through research, more therapies and more ways to support families.”