MeSH 搜索器

Gonadal Dysgenesis, 46,XY

Defects in the SEX DETERMINATION PROCESS in 46, XY individuals that result in abnormal gonadal development and deficiencies in TESTOSTERONE and subsequently ANTIMULLERIAN HORMONE or other factors required for normal male sex development. This leads to the development of female phenotypes (male to female sex reversal), normal to tall stature, and bilateral streak or dysgenic gonads which are susceptible to GONADAL TISSUE NEOPLASMS. An XY gonadal dysgenesis is associated with structural abnormalities on the Y CHROMOSOME, a mutation in the GENE, SRY, or a mutation in other autosomal genes that are involved in sex determination.
推出的年份: 1991(1980)
副标题
树号: C12.050.351.875.253.096.687, C12.050.351.875.253.309.388, C12.200.706.316.096.687, C12.200.706.316.309.388, C12.800.316.096.687, C12.800.316.309.388, C16.131.939.316.096.687, C16.131.939.316.309.388, C19.391.119.096.687, C19.391.119.309.388
MeSH 单一 ID: D006061
进入的组:
  • Sex Reversal, Gonadal, 46, XY
  • Gonadal Dysgenesis, 46, XY
  • 46, XY Gonadal Dysgenesis
  • 46, XY Gonadal Sex Reversal
  • Swyer Syndrome
  • Syndrome, Swyer
  • Pure Gonadal Dysgenesis 46,XY
  • 46,XY Complete Gonadal Dysgenesis
  • XY Pure Gonadal Dysgenesis
  • Complete Gonadal Dysgenesis, 46, XY
  • Pure Gonadal Dysgenesis, 46, XY
早前的内容:
  • Sex Differentiation Disorders (1966-1979)
  • Turner's Syndrome (1967-1979)

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