A mother in Bay City is on a mission to create more inclusivity and awareness for those with special needs.  This is to honor ...

A person may have Angelman syndrome symptoms because parts of the UBE3A gene are inactive or missing – which happens in around 70 per cent of cases. Structural changes to UBE3A also result in ...

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

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

Shortly thereafter, diagnoses of Angelman syndrome began to rise. Today, the disorder is known to occur in approximately one in every 15,000 to 20,000 people, and it has been reported all over the ...

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 ...

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.

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 ...

Doctors eventually diagnosed Colin with Angelman syndrome after genetic testing showed he had a rare chromosomal mutation. "With the diagnosis also came a little bit of relief because we at ...