Turner syndrome
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British pronunciation/tˈɜːnəz sˈɪndɹəʊm/
American pronunciation/tˈɜːnɚz sˈɪndɹoʊm/
turner's syndrome

Definição e Significado de "turner syndrome"

Turner syndrome
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síndrome de Turner, síndrome de Turner (condição genética)

a genetic condition affecting females, where one of the X chromosomes is partially or completely missing, leading to various developmental and medical challenges

What is "turner syndrome"?

Turner syndrome is a genetic condition that affects females and is typically characterized by the absence of all or part of one of the X chromosomes. It is associated with a range of physical features such as being short, having excess skin folds on the side of the neck, low hairline at the back of the neck, and a broad chest with widely spaced nipples. Individuals with Turner syndrome may also experience developmental delays, especially in movement abilities, as well as reproductive issues, such as infertility or early menopause. Additionally, they may have certain medical conditions, including heart problems, kidney problems, and thyroid disorders. Treatment for Turner syndrome may involve growth hormone therapy to increase height, estrogen replacement therapy to start puberty and support bone health, and medical treatments for specific health problems.

turner syndrome

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Individuals with Turner syndrome typically have short stature and a lack of normal pubertal development.
Turner syndrome is caused by the absence of part or all of one of the X chromosomes.
Turner syndrome occurs in approximately 1 in 2,500 live female births.
Turner syndrome can be associated with various health issues, including heart and kidney abnormalities.
Educational and psychosocial support is essential for individuals with Turner syndrome.
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