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Turner syndrome, a condition that affects only females, results when one of the x chromosomes (sex chromosomes) is missing or partially missing Sometimes, it may be diagnosed during adolescence in those with milder symptoms. Turner syndrome can cause a variety of medical and developmental problems, including short height, failure of the ovaries to develop and heart defects.
Turner syndrome (ts), commonly known as 45,x, or 45,x0, [note 1] is a chromosomal disorder in which cells of females have only one x chromosome instead of two, or are partially missing an x chromosome (sex chromosome monosomy) leading to the complete or partial deletion of the pseudoautosomal regions (par1, par2) in the affected x chromosome The diagnosis might come shortly after birth or in early childhood Turner syndrome is caused by genetic mutations, also known as pathogenic variants
Genetic mutations can be hereditary, when parents pass them down to their children, or they may occur randomly when cells are dividing.
Turner syndrome can cause symptoms and complications throughout life, but treatments allow girls and women with this rare genetic disease to live relatively healthy lives. There's no cure for turner syndrome, but certain treatments can help cope with the symptoms and effects of this condition Hormone treatments with growth hormone and/or other hormones can improve growth and help girls achieve taller heights in adulthood. Turner syndrome happens in females when one x chromosome is missing or partially missing
Learn about the types, symptoms, diagnosis, and treatment.
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