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  2. Turner syndrome - Wikipedia

    en.wikipedia.org/wiki/Turner_syndrome

    Specific autoimmune disorders linked to Turner syndrome include Hashimoto's disease, vitiligo, psoriasis and psoriatic arthritis, alopecia,Type I diabetes, and celiac disease Type I diabetes, when the immune system attacks the beta cells in the pancreas, is a major autoimmune disorder and is much more common in Turner females than 46,XX and 47 ...

  3. Hypergonadotropic hypogonadism - Wikipedia

    en.wikipedia.org/wiki/Hypergonadotropic_hypogonadism

    Hypergonadotropic hypogonadism can be caused by a variety of genetic and acquired factors. Common genetic causes include Turner syndrome and Klinefelter syndrome, while acquired causes may involve infections, trauma, radiation, or chemotherapy affecting the gonads. [13]

  4. Hypogonadism - Wikipedia

    en.wikipedia.org/wiki/Hypogonadism

    Examples of congenital causes of hypogonadism, that is, causes that are present at birth: [citation needed] Turner syndrome and Klinefelter syndrome. It is also one of the signs of CHARGE syndrome. Examples of acquired causes of hypogonadism: [citation needed]

  5. Disorders of sex development - Wikipedia

    en.wikipedia.org/wiki/Disorders_of_sex_development

    Turner syndrome (Ullrich-Turner syndrome and gonadal dysgenesis) – a condition that describes a female born with only one X chromosome or with an abnormal X chromosome, making her karotype 45,X0. It occurs in 1 in 2,000 to 5,000 females. [ 61 ]

  6. Gonadal dysgenesis - Wikipedia

    en.wikipedia.org/wiki/Gonadal_dysgenesis

    Turner syndrome is usually not diagnosed until a delayed onset of puberty with Müllerian structures found to be in infantile stage. [4] Physical phenotypic characteristics include short stature, dysmorphic features and lymphedema at birth. [23] Comorbidities include heart defects, vision and hearing problems, diabetes, and low thyroid hormone ...

  7. Wilson–Turner syndrome - Wikipedia

    en.wikipedia.org/wiki/Wilson–Turner_syndrome

    It can also cause short stature in men and women. In addition to little genital development, pubic and body hair are scant. [7] Some of the facial features that are associated with Wilson–Turner syndrome include small head circumferences, high foreheads, prominent ears, and noses with flattened bridges.

  8. 45,X/46,XY mosaicism - Wikipedia

    en.wikipedia.org/wiki/45,X/46,XY_mosaicism

    The observable characteristics of this condition are highly variable, ranging from gonadal dysgenesis in males, to Turner-like females and phenotypically normal males. [6] The phenotypical expression may be ambiguous, male or female, regardless of the extent of the mosaicism . [ 7 ]

  9. Monosomy - Wikipedia

    en.wikipedia.org/wiki/Monosomy

    Human conditions due to monosomy: Turner syndromeFemales with Turner syndrome typically have one X chromosome instead of the usual two X chromosomes. Turner syndrome is the only full monosomy that is seen in humans — all other cases of full monosomy are lethal and the individual will not survive development.