An insurance company has denied newborn twins a one-time genetic treatment that could stop the progression of their spinal ...

Affecting an estimated one in 12,000 baby girls born each year (and only rarely seen in boys), this genetic disorder causes ...

Bridget Finn’s daughter, Flo, was born with a rare genetic mutation, STXBP1 — but the family has put their "grief" into action with a powerful fundraising effort.

Tourette disorder is a disorder of the nervous system that affects children, adolescents and adults. The condition is ...

First linked to mutations in the CHD7 gene in 2004, CHARGE syndrome is a rare genetic disorder occurring in approximately 1 in 8,500 to 15,000 births. According to the National Institute of Health ...

Recent research indicates that people with two copies of the APOE4 gene are almost certain to exhibit signs of the ...

Research led by Prof. Shani Stern at the University of Haifa unveils genetic discrepancies in schizophrenia discordant ...

Chandigarh doctors help thalassemia couple deliver baby without the genetic disorder using breakthrough procedure ...

The research focused on a variant called APOE4 and largely looked at people of European ancestry—risk levels are different ...

In research that may be a step forward toward finding personalized treatments for Tourette disorder, scientists at Rutgers University–New Brunswick have bred mice that exhibit some of the same ...

People who carry two copies of the gene mutation most strongly implicated in Alzheimer's disease are almost certain to ...

OTC deficiency is the most common urea cycle disorder and is caused by a genetic defect in a liver enzyme responsible for the detoxification of ammonia. The Fast Track designation is designed to begin ...