Related: Colin Farrell Starts Foundation in Honor of Son with Angelman Syndrome as He Opens Up About Their Life (Exclusive) ...

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

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

The plan comes just ahead of the presentation of detailed data from the phase 1/2 HALOS study ION582 – also known as BIIB121 – at the 2024 Angelman Syndrome Foundation (ASF) family conference ...

Ms Cross said the foundation was focused on research while offering support to parents and carers of children with Angelman syndrome. "The hole in your heart will always be there," she said.

It all started with a mother who couldn’t help but notice that her baby was failing to reach important milestones in his development. “Don’t worry,” ...

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?

"Angelman Syndrome is a neurogenetic disorder," said Weston's mother Felicia Warner. "It affects a lot of different things. It affects their balance, a very high percentage has seizures ...

Colin Farrell Dedicates New Foundation To Son Suffering From Angelman Syndrome: All Because Of James... At Least 30 Infants In US Born With Fetal Fentanyl Syndrome; Know Everything About This ...

Monica LaMura had never heard of Angelman syndrome until her youngest son was diagnosed with the rare neurogenetic condition in December. LaMura described her pregnancy and life with Colin, who is ...