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MeSH 搜索器

Klinefelter Syndrome

A form of male HYPOGONADISM, characterized by the presence of an extra X CHROMOSOME, small TESTES, seminiferous tubule dysgenesis, elevated levels of GONADOTROPINS, low serum TESTOSTERONE, underdeveloped secondary sex characteristics, and male infertility (INFERTILITY, MALE). Patients tend to have long legs and a slim, tall stature. GYNECOMASTIA is present in many of the patients. The classic form has the karyotype 47,XXY. Several karyotype variants include 48,XXYY; 48,XXXY; 49,XXXXY, and mosaic patterns ( 46,XY/47,XXY; 47,XXY/48,XXXY, etc.).
推出的年份:
副标题
树号: C12.050.351.875.253.795.500, C12.200.706.316.795.500, C12.800.316.795.500, C16.131.260.830.835.500, C16.131.939.316.795.500, C16.320.180.830.835.500, C19.391.119.795.500, C19.391.482.629
MeSH 单一 ID: D007713
进入的组:
  • Klinefelter Syndromes
  • Syndrome, Klinefelter
  • Syndromes, Klinefelter
  • XXY Syndrome
  • Syndrome, XXY
  • Syndromes, XXY
  • XXY Syndromes
  • Klinefelter's Syndrome
  • Klinefelters Syndrome
  • Syndrome, Klinefelter's
  • Klinefelter Syndrome, Variants
  • Klinefelter Syndromes, Variants
  • Syndrome, Variants Klinefelter
  • Syndromes, Variants Klinefelter
  • 48,XXYY Syndrome
  • Xxyy Syndrome
  • Syndrome, Xxyy
  • Syndromes, Xxyy
  • Xxyy Syndromes
  • XXY Trisomy
  • Trisomies, XXY
  • Trisomy, XXY
  • XXY Trisomies
  • 49,XXXXY Syndrome
  • XXXY Males
  • XXXY Male

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