Hollywood actor Colin Farrell recently opened up on his son James – diagnosed with a rare genetic condition Angelman Syndrome, in childhood. The Phonebooth actor revealed that James, 20 suffers ...

Colin Farrell shares photos and talks about his son James, 20, who has Angelman syndrome. Farrell is starting a foundation to help. “I want the world to be kind to James." ...

Angelman syndrome is a rare disease that disrupts the normal development and function of cells, particularly in the nervous system, leading to severe developmental delays and learning disabilities.

For the first time, Colin Farrell has opened up his home and talked in-depth about life with his son James, who has Angelman syndrome. James was just a toddler when he was diagnosed with the rare ...

It is named after Dr. Harry Angelman, and English physician who first described the condition in 1965. The disorder is rare, affecting around one in 12,000 to 20,000 people, the Cleveland Clinic ...

Colin Farrell opened up to PEOPLE about his son James, who was diagnosed with Angelman syndrome. Here’s what to know about the rare neurogenetic disorder that affects 1 in 15,000 people.

Actor Colin Farrell is launching a new foundation to raise awareness of a rare genetic condition called Angelman syndrome, so that his son and others with the disorder will have more support and ...

Colin Farrell's 20-year-old son, James, was diagnosed with Angelman syndrome, ... Getty Images for National Board of Review. You are viewing 1 of 5 images Previous Image Next Image.

Ultragenyx reports early success with Angelman syndrome drug, backing up 2022 acquisition. By Allison DeAngelis April 15, 2024. Reprints. David Goldman/AP.

The rare neurogenetic disorder affects 1 in 15,000 people. 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 actor’s son James has Angelman syndrome, a rare neurogenetic disorder. The Colin Farrell Foundation aims to raise awareness about intellectual disability.

Angelman syndrome is a rare disease that disrupts the normal development and function of cells, particularly in the nervous system, leading to severe developmental delays and learning disabilities.