Turner syndrome occurs when one of the X chromosomes (sex chromosomes) is absent or partly missing, affecting only females. Turner syndrome may result in a number of medical and physical problems, such as short stature, ovarian failure, and heart defects.

Turner syndrome may be detected before birth (early in pregnancy), during childhood, or in early adolescence. The diagnosis of Turner syndrome in females with moderate signs and symptoms is often delayed until they are in their adolescent or young adult years.

Turner syndrome affects both girls and women, and they need constant medical treatment from a number of specialists. Most girls and women will live stable, independent lives with routine care and proper treatment.
Turner syndrome genotypes

The most common genotype of Turner syndrome is 45, X

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