The heartbroken family of a young man who died while training for a white-collar boxing charity match have spoken out in fury ...

This feature first ran in a special publication called Hometown Pride, published June 28, 2025, featuring people and ...

Angelman syndrome (AS) is a rare neurodevelopmental disorder caused by the loss of function of the maternally inherited ubiquitin E3 ligase UBE3A gene. AS is characterized by severe symptoms, ...

Marathon runner covers 1100km across NSW to raise awareness for Angelman Syndrome and Huxley’s Heroes ...

Broken Hill man Mitch McKenny plans to run from the outback city to Newcastle in 29 days. He aims to raise awareness and funds for Angelman syndrome, a rare genetic disorder. Tradie 'fed up' as ...

Cincinnati native Charlie Nuck has a 6-year-old niece named Briar. She has a rare, neurogenetic disorder called Angelman syndrome. It affects about one in 15,000 people and causes developmental delays ...

According to DelveInsight's estimates, the Angelman syndrome market size in the 7MM is expected to show positive growth during the forecast period (2025–2034), primarily driven by the increasing ...

3-year-old Bellamy Bresaw of Bow was diagnosed with Angelman Syndrome at nine months old. Credit: Delores Flanders / Courtesy Delores Flanders and her family are hosting a fundraiser at Boutwell’s ...

MIDDLETON, Mass., May 12, 2025 /PRNewswire/ -- MavriX Bio, a clinical-stage biotechnology company focused on the development of transformative genetic therapies for Angelman syndrome (AS), today ...

SARASOTA, Fla. and NOVATO, Calif., Jan. 15, 2020 (GLOBE NEWSWIRE) -- GeneTx Biotherapeutics LLC and Ultragenyx Pharmaceutical Inc. (NASDAQ: RARE), a biopharmaceutical company focused on the ...

BAY CITY, Mich. (WJRT) - A mother in Bay City is on a mission to create more inclusivity and awareness for those with special needs. This is to honor her five-year-old son, who has Angelman Syndrome, ...