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 chromosomal condition involving a person’s sex chromosomes. It is considered mosaic when an X chromosome is missing in some cells in people who have two X chromosomes. Share ...

Turner syndrome is a condition in which a female is missing all or part of one X chromosome. Normally, people have two sex chromosomes in each cell: Females have two X chromosomes, and males have ...

Turner syndrome is a genetic condition in which a (female) person has only one X chromosome instead of two. ... (DSDs) can result in mixed or ambiguous sex-related physical characteristics, ...

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 is a rare genetic condition that only affects females. It occurs when one of the two X chromosomes that should be present in a female’s body is missing or does not function ...

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

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 ...

She then started the Idaho Turner Syndrome Foundation, which put her in touch with Jacquelyn Wooldridge. "There are many women and girls who feel that they are the only ones," Wooldridge said.