Broken Hill steps up for the family of a boy born with a rare and debilitating genetic condition. But none will go further ...

Kristi Hill-Herrera shares her experience with The Arc of San Antonio, which has been instrumental in supporting her daughter ...

HEMLOCK, Mich. (WJRT) - A Saginaw County community came together for 6-year-old Weston Mejia, who was born with a rare genetic condition known as Angelman Syndrome. His family is in the ...

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

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

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

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 ...

SINGAPORE – Laughter fills the consultation room whenever Lucas Oon, 17, is with the team managing his care – paediatric neurologist Jeremy Lin, assistant nurse clinician Kimberly Quek and ...

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.

Telling stories through natural beauty has been a hallmark of Haines’s work as a floral and landscape designer for more than ...

The Association of Parents of Persons with Intellectual Disabilities of Thailand (APID) invites interested people to see beautiful artworks created by young artists with Down syndrome during ...