Angelman syndrome, which affects 1 in 15,000 people, is a rare neurogenetic disorder that stems from a mutation or deletion of a gene in the 15th chromosome, called the ubiquitin protein ligase ...

Angelman syndrome is a rare neuro-genetic disorder caused by a loss of function of the UBE3A gene that happens during fetal development, and causes developmental delays, intellectual disability ...

Actor Colin Farrell publicizes that his son, James, has Angelman Syndrome. Here's what Angelman Syndrome is, and if a cure is ...

Angelman syndrome is a rare neurogenetic disorder affecting approximately 1 in 15,000 live births or 500,000 people globally. It results from the loss of function of the UBE3A gene located on the ...

New approach finds ‘parent-of-origin’ effects in more than a dozen genes — without the need for parental data.

People with Angelman syndrome have sleep problems including abnormal sleeping cycles or less need for sleep. Seizures often begin between ages 18 months and 3 years.

Two-year-old Cami Thompson is quick to smile and laugh. But her joy is actually a symptom of Angelman syndrome, a rare, incurable, neuro-genetic disorder that affects the 15th chromosome.

Millie, who lives with Angelman syndrome, has just learnt to walk, but is it fair for me to use technology to render a ...

Colin Farrell Reveals Son James Lives With Rare Disorder During a new interview, the actor revealed that his son has been living with a genetic disorder. Learn more about Angelman Syndrome, here.

Cyclists led by Charlie Nuck will arrive in Bar Harbor Saturday to raise awareness and funds for the rare neurogenetic ...

Angelman syndrome, which affects 1 in 15,000 people, is a rare neurogenetic disorder that stems from a mutation or deletion of a gene in the 15th chromosome, called the ubiquitin protein ligase E3A ...