Brecon, known as Brecs, was born with dup15q syndrome, a rare chromosome disorder that has caused uncontrolled epilepsy, autism, profound learning disability, osteoporosis, sensory processing ...

Prader-Willi syndrome is caused by changes in gene expression in a specific portion of chromosome 15. Starting in childhood, it often leads to extreme, insatiable hunger.(Image credit: Catherine ...

"A genetic test confirmed she has Dup15q syndrome, which is caused by an extra piece of a chromosome," said mom Jackie Vanderhoof. Fiona Vanderhoof is developmentally delayed and mostly nonverbal.

His team has been studying the two rare, genetic disease syndromes that also result in profound autism, Dup15q Syndrome and Angelman Syndrome. They impact about 1 in 5,000 children.

Quiver Bioscience Inc. is collaborating with the Dup15q Alliance to advance an antisense oligonucleotide (ASO) therapeutic program for chromosome 15q duplication (Dup15q) syndrome.

CAMBRIDGE, Mass.-- (BUSINESS WIRE)-- Quiver Bioscience (“Quiver”), a discovery technology and therapeutics company advancing programs for the treatment of serious central nervous system (CNS) ...

There are currently no disease-modifying treatments for Dup15q, which remains a substantial unmet medical need. Javascript is required for you to be able to read premium content.

Quiver Bioscience (“Quiver”), a discovery technology and therapeutics company advancing programs for the treatment of serious central nervous system (CNS) disorders, announces today a collaboration ...

To start, his team has been studying two rare, genetic disease syndromes that also result in profound autism, Angelman Syndrome and Dup15q Syndrome. They impact about 1 in 5,000 children. While it ...

To start, his team has been studying two rare, genetic disease syndromes that also result in profound autism, Angelman Syndrome and Dup15q Syndrome. They impact about 1 in 5,000 children.