MeSH 搜索器

De Lange Syndrome

A syndrome characterized by growth retardation, severe MENTAL RETARDATION, short stature, a low-pitched growling cry, brachycephaly, low-set ears, webbed neck, carp mouth, depressed nasal bridge, bushy eyebrows meeting at the midline, hirsutism, and malformations of the hands. The condition may occur sporadically or be associated with an autosomal dominant pattern of inheritance or duplication of the long arm of chromosome 3. (Menkes, Textbook of Child Neurology, 5th ed, p231)
推出的年份: 2000(1964)
副标题
树号: C10.597.606.360.210, C16.131.077.272, C16.131.260.210, C16.320.180.210
MeSH 单一 ID: D003635
进入的组:
  • Cornelia De Lange Syndrome
  • Brachmann-De Lange Syndrome
  • Brachmann De Lange Syndrome
  • Syndrome, Brachmann-De Lange
  • Typus Degenerativus Amstelodamensis
  • Amstelodamensis, Typus Degenerativus
  • De Lange's Syndrome
  • Cornelia de Lange Syndrome 2
  • CdLS, X-Linked
  • CdLS, X Linked
  • CdLSs, X-Linked
  • X-Linked CdLS
  • X-Linked CdLSs
  • CdLS2
  • Cornelia de Lange Syndrome, X-Linked
  • Cornelia de Lange Syndrome, X Linked
  • Cornelia de Lange Syndrome 3
  • Cornelia de Lange Syndrome 1

留言 (0)

沒有登入
gif