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.

What Is Turner Syndrome? 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 ...

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. Only people ...

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 condition in which a woman is missing all or part of one X chromosome. It is sometimes treated with hormones and therapy.

Turner Syndrome is a rare genetic disorder that impacts women. According to the Turner Syndrome Foundation, about 1 in 2,000 women are affected by the syndrome.

Turner syndrome is a genetic condition in which a (female) person has only one X chromosome instead of two. Scientists have used a new computational method for precisely measuring sex chromosomes ...

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.

Turner syndrome 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: ...