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

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

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?

Lucas Oon has Angelman syndrome, which is characterised by a happy demeanour and an easily excitable nature. Read more at ...

The date reflects the genetic defect Angelman Syndrome causes in the 15th chromosome and nods to Feburary’s designation as Rare Disease Month.

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 ...

Laughing is one of the better-known traits of Angelman syndrome, a rare neurogenetic disorder that disrupts typical messaging in the brain. A single missing gene leads to the absence of a vital ...

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 ...

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 ...