MeSH 搜索器

Primary Ovarian Insufficiency

Cessation of ovarian function after MENARCHE but before the age of 40, without or with OVARIAN FOLLICLE depletion. It is characterized by the presence of OLIGOMENORRHEA or AMENORRHEA, elevated GONADOTROPINS, and low ESTRADIOL levels. It is a state of female HYPERGONADOTROPIC HYPOGONADISM. Etiologies include genetic defects, autoimmune processes, chemotherapy, radiation, and infections. The most commonly known genetic cause is the expansion of a CGG repeat to 55 to 199 copies in the 5' untranslated region in the X-linked FMR1 gene.
推出的年份: 2011(1992)
副标题
树号: C12.050.351.500.056.630.750, C12.100.250.056.630.750, C19.391.630.750
MeSH 单一 ID: D016649
进入的组:
  • Ovarian Insufficiency, Primary
  • Ovarian Failure, Premature
  • Premature Ovarian Failure
  • Gonadotropin-Resistant Ovary Syndrome
  • Gonadotropin Resistant Ovary Syndrome
  • Resistant Ovary Syndrome
  • Hypergonadotropic Ovarian Failure, X-Linked
  • Hypergonadotropic Ovarian Failure, X Linked
  • X-Linked Hypergonadotropic Ovarian Failure
  • X Linked Hypergonadotropic Ovarian Failure
  • Premature Ovarian Failure, X-Linked
  • Premature Ovarian Failure, X Linked
  • Fragile X-Associated Primary Ovarian Insufficiency
  • Fragile X Associated Primary Ovarian Insufficiency
  • Fragile X Premature Ovarian Failure
  • FMR1-Related Primary Ovarian Insufficiency
  • FMR1 Related Primary Ovarian Insufficiency
  • Primary Ovarian Insufficiency, Fragile X-Associated
  • Primary Ovarian Insufficiency, Fragile X Associated
  • Premature Ovarian Failure 1
早前的内容:
  • Menopause, Premature (1975-1991)
  • Ovarian Diseases (1966-1991)

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