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

It's confirmed through a genetic blood test. Once officially diagnosed, early intervention is key. Although there is no cure ...

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

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.

We each get two copies of every gene - one copy from each of our parents. But what happens when one of these genes has been "turned off", or imprinted, and the remaining gene is defective?

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

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.

Lucas has Angelman syndrome (AS), a rare neurogenetic condition ... READ: Spinal Muscular Atrophy: Genetic disease that kills, maims kids but with no testing capability in PH “Lucas’ case ...

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 ...

Know Everything About This Condition Angelman syndrome, also known as AS, is a genetic disorder that affects the nervous system and causes developmental and neurological problems. According to ...