Turner syndrome is a genetic disorder exclusive to the female sex in which an X chromosome is either partially or entirely missing. Here's what you should know about it.

Turner syndrome is a rare genetic disorder found in some women and people assigned female at birth. It can cause short stature and a range of health issues including heart defects, learning ...

Turner syndrome is a genetic condition caused by an abnormality on one of your sex chromosomes. It’s also called monosomy X, gonadal dysgenesis, and Bonnevie-Ullrich syndrome.

Turner Syndrome (TS) is a rare genetic condition that affects approximately 1 in every 2,500 female births worldwide. While it might not be widely known, its impact on those who have it can be ...

Turner Syndrome. Genetic and Rare Diseases Information Center. February 2023. Life Expectancy. Centers for Disease Control and Prevention. February 7, 2023.

CHERRY VALLEY (WREX) — Many were out on their bikes Saturday, raising awareness for a rare genetic disorder. Bikers came together at Kegel Harley-Davidson in Cherry Valley Saturday morning for ...

The genetic analysis showed that some cells had one X chromosome and others had the usual two, known as mosaic Turner syndrome. Women with Turner syndrome generally undergo human growth hormone ...

Roughly 2,500-year-old DNA has revealed the first ancient person on record with Turner syndrome, a genetic condition in which a person has just a single X chromosome rather than two, a new study ...

Around 1 in every 2,500 female births is affected by Turner syndrome. In Idaho, 481 women and girls have this genetic disorder, according to the Turner Syndrome Foundation.