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 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 (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 ...

Prenatal Testing for Turner Syndrome. Your doctor can perform one of two tests to make a diagnosis before your baby’s birth: ... Turner syndrome clinic, and general genetics clinic, ...

Genetic testing for muscular dystrophy is important because it can help determine which of the more than 30 types you have. ... Turner syndrome clinic, and general genetics clinic, ...

An NT scan, or nuchal translucency scan, is a non-invasive ultrasound screening for Down syndrome and other genetic conditions during pregnancy. It’s usually done between weeks 11 and 14 of ...

Rett syndrome is a rare developmental disorder, most often due to a mutation in the MECP2 gene on the X chromosome, but it’s not usually inherited. Advances in genetics have launched a new era ...

Genetic testing to identify women with Lynch Syndrome is likely to need to increase dramatically to ensure that carriers are not missed, a new analysis has found. A study by The Institute of Cancer ...

Turner syndrome is a genetic condition with no cure, but treatment may help resolve issues with short stature, sexual development, and learning difficulties. Early preventive care is important to ...

Parsonage-Turner syndrome (PTS) is a condition that affects certain nerves in the upper body. Doctors also call it brachial plexitis or brachial neuritis. The characteristic feature of PTS is ...