1p36 deletion syndrome is one of the most common subtelomeric microdeletion disorders, occurring in approximately 1 in 5,000 to 10,000 live births. This chromosomal abnormality results in a broad ...

22q11.2 Deletion Syndrome (22q11.2 DS) is the most common chromosomal microdeletion disorder, arising chiefly from de novo non-homologous meiotic recombination events. This condition presents with a ...

Zynerba Pharmaceuticals, Inc. ZYNE presented positive long-term 38-week data from the phase 2 INSPIRE trial with Zygel in children and adolescents with 22q11.2 deletion syndrome. The data were ...

Researchers at Baylor College of Medicine, the Jan and Dan Duncan Neurological Research Institute (Duncan NRI) at Texas Children's Hospital, Baylor Genetics and collaborating institutions provided a ...

LAS VEGAS, Nev. (FOX5) -The parents of Niko Gastelum nicknamed their son baby “Incredible Hulk” because of all he’s endured dealing with a rare genetic disorder called 5q31.3 Microdeletion Syndrome.

Researchers at Baylor College of Medicine, the Jan and Dan Duncan Neurological Research Institute (Duncan NRI) at Texas Children's Hospital, Baylor Genetics and collaborating institutions provided a ...

As a pastor, I’ve wrestled with the theological implications of my child’s disability. When my nine-year-old son Benji was an infant, we were in and out of hospitals for the first few months of his ...

Researcher discovers possible link of mitochondrial function to the development of schizophrenia. Researchers at Rutgers and Emory University are gaining insights into how schizophrenia develops by ...