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WASHINGTON — Terry Jo Bichell earned a master’s degree in public health, became an expert in pregnancy-related deaths, and made documentary films about women’s health projects in Côte d’Ivoire, Gambia, Nigeria and Senegal. But nothing prepared her for the news that her baby, Louie, had Angelman syndrome. It was 17 years…

People with Angelman syndrome and other rare diseases need more psychosocial support, an Oregon State University study reports. A lot of the support can be similar, cutting across the types of disorders that patients have, the team said. It’s common for people with rare diseases to have more anxiety, depression, pain and…

Mutations in the VARS2 gene, which is involved in mitochondrial function, may lead to an Angelman syndrome-like disorder, according to a case report published in the journal Human Genomics. The case was presented by a research team at King Faisal Specialist Hospital and Research Centre in Riyadh, Saudi Arabia,…

The U.S. Food and Drug Administration (FDA) awarded a fast track designation to Ovid Therapeutics’ OV101 for the treatment of Angelman syndrome. The designation allows for expedited development and review of therapeutics for serious diseases with high unmet medical need. “This designation is an important milestone for both Ovid…

A group of designers from around the world will be showcasing their latest designs on April 28, 2018, in New York City while the Foundation for Angelman Syndrome Therapeutics (FAST) raises funds to support research for a cure for Angelman syndrome (AS). Credit: Katherine Angelique…

Ovid Therapeutics presented data from several studies that support the clinical development of the investigational therapy TAK-935/OV935 as a potential treatment for developmental and epileptic encephalopathies. These results are particularly significant for Angelman syndrome patients, 85 percent of whom suffer from some form of epilepsy. The findings from…