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

Riddhi believes that despite biological markers being passed on, it’s also important that parents tweak the way they behave with their kids or in front of their kids. She opines that if as a child ...

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 ...

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.

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 ...

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.

Angelman syndrome is a rare genetic condition that affects the nervous system and causes severe physical and learning disabilities. Sarah said continuing to work as a solicitor had given her a sense ...

Angelman syndrome and Prader-Willi syndrome highlight the importance of investigating genetic conflict's influence on psychology and behavior. Researchers have documented differences in ...

Hundreds of people are expected to help shine a light on rare illnesses by taking part in the Rare Disease Fun Run on Sunday, ...