Broken Hill steps up for the family of a boy born with a rare and debilitating genetic condition. But none will go further ...

Families in Connecticut and beyond are looking for answers when it comes to treating Angelman Syndrome, but fear funding ...

Ionis and Ultragenyx are competing to develop oligonucleotide treatments for Angelman syndrome, but will Neuren’s peptide ...

BAY CITY, Mich. (WJRT) - A mother in Bay City is on a mission to create more inclusivity and awareness for those with special ...

Angelman syndrome is caused by a large deletion of the region of the maternal chromosome that contains UBE3A, or by a DNA sequence change (mutation) in the UBE3A gene inherited from the mother.

Kristi Hill-Herrera shares her experience with The Arc of San Antonio, which has been instrumental in supporting her daughter ...

This is a five-month-old baby girl diagnosed with Angelman Syndrome. Disclaimer: AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing ...

Ionis has committed to a phase 3 programme for its antisense therapy for rare genetic disorder Angelman syndrome, just weeks after Biogen decided against exercising an option to license the drug.

Considering taking supplements to treat angelman syndrome? Below is a list of common natural remedies used to treat or reduce the symptoms of angelman syndrome. Follow the links to read common ...

MONTROSE, Mich. (WJRT) - A Mid-Michigan family is raising money to help their 6-year-old boy with a rare genetic disorder. After spending a few months looking for action figures and fun items, Kristin ...

Monica LaMura had never heard of Angelman syndrome until her youngest son was diagnosed with the rare neurogenetic condition in December. LaMura described her pregnancy and life with Colin ...