Turner syndrome (Q202849)

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chromosomal variation where a person is born with a 45X chromosome pattern rather than the typical 46XX
  • Bonnevie-Ullrich syndrome
  • Bonnevie-Ullrich syndrome NOS
  • Bonnevie-Ullrich syndrome NOS (disorder)
  • Gonadal dysgenesis - Turner
  • Karyotype 45, X
  • Monosomy X
  • Turner syndrome (disorder)
  • Turner's syndrome NOS
  • Turner's syndrome NOS (disorder)
  • XO syndrome
  • monosomy X syndrome
  • Ullrich–Turner syndrome
  • Turner's syndrome
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Language Label Description Also known as
English
Turner syndrome
chromosomal variation where a person is born with a 45X chromosome pattern rather than the typical 46XX
  • Bonnevie-Ullrich syndrome
  • Bonnevie-Ullrich syndrome NOS
  • Bonnevie-Ullrich syndrome NOS (disorder)
  • Gonadal dysgenesis - Turner
  • Karyotype 45, X
  • Monosomy X
  • Turner syndrome (disorder)
  • Turner's syndrome NOS
  • Turner's syndrome NOS (disorder)
  • XO syndrome
  • monosomy X syndrome
  • Ullrich–Turner syndrome
  • Turner's syndrome

Statements

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45,X.jpg
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XO kariotipoa (Basque)
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Turner syndrome
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Identifiers

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Turnerův syndrom
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Turner Syndrome
A syndrome of defective gonadal development in phenotypic females associated with the karyotype 45,X (or 45,XO). Patients generally are of short stature with undifferentiated gonads (streak gonads), sexual infantilism, hypogonadism, webbing of the neck, cubitus valgus, elevated gonadotropins, decreased estradiol level in blood, and congenital heart defects. noonan syndrome (also called Pseudo-Turner Syndrome and Male Turner Syndrome) resembles this disorder; however, it occurs in males and females with a normal karyotype and is inherited as an autosomal dominant. (English)
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LD50.0
Turner syndrome
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Turner syndrome
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Turnerin oireyhtymä
Turners syndrom
Turner's syndrome
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