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

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 is a genetic disorder affecting females, characterized by the partial or complete absence of one of the two X chromosomes. It leads to symptoms including: short stature; ...

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 ...

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 ...

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 ...

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.