MeSH 搜索器

Rothmund-Thomson Syndrome

An autosomal recessive syndrome occurring principally in females, characterized by the presence of reticulated, atrophic, hyperpigmented, telangiectatic cutaneous plaques, often accompanied by juvenile cataracts, saddle nose, congenital bone defects, disturbances in the growth of HAIR; NAILS; and TEETH; and HYPOGONADISM.
推出的年份: 2006(1964)
副标题
树号: C16.131.831.775, C16.320.850.765, C16.614.760, C17.800.804.775, C17.800.827.775, C18.452.284.760
MeSH 单一 ID: D011038
进入的组:
  • Rothmund Thomson Syndrome
  • Syndrome, Rothmund-Thomson
  • Poikiloderma Congenitale of Rothmund-Thomson
  • Poikiloderma Atrophicans and Cataract
  • Congenital Poikiloderma
  • Poikiloderma Congenitale
  • Congenitale, Poikiloderma
  • Congenitales, Poikiloderma
  • Poikiloderma Congenitales
  • Poikiloderma of Rothmund-Thomson
  • Poikiloderma of Rothmund Thomson
  • Rothmund-Thomson Poikiloderma
  • Rothmund-Thomson Poikilodermas

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