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Concept information

Preferred term

De Lange Syndrome  

Type

  • Topical Descriptor

Entry terms

  • Amstelodamensis, Typus Degenerativus
  • Brachmann De Lange Syndrome
  • Brachmann-De Lange Syndrome
  • Cornelia De Lange Syndrome
  • De Lange's Syndrome
  • Syndrome, Brachmann-De Lange
  • Typus Degenerativus Amstelodamensis

Scope note

  • 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)

History note

  • 2000(1964)

In other languages

  • Finnish

  • Cornelia de Lange
  • Cornelia de Langen syndrooma
  • de Lange
  • De Langen oireyhtymä
  • de Langen syndrooma
  • syndroma de Lange
  • Swedish

  • Brachmann-de Langes syndrom
  • Cornelia de Langes syndrom

URI

http://www.yso.fi/onto/mesh/D003635

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