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Concept information

Preferred term

Rubinstein-Taybi Syndrome  

Type

  • mesh:Descriptor

Definition

  • A chromosomal disorder characterized by MENTAL RETARDATION, broad thumbs, webbing of fingers and toes, beaked nose, short upper lip, pouting lower lip, agenesis of corpus callosum, large foramen magnum, keloid formation, pulmonary stenosis, vertebral anomalies, chest wall anomalies, sleep apnea, and megacolon. The disease has an autosomal dominant pattern of inheritance and is associated with deletions of the short arm of chromosome 16 (16p13.3).

Entry terms

  • Broad Thumb-Hallux Syndrome
  • Broad Thumbs and Great Toes, Characteristic Facies, and Mental Retardation
  • Rubinstein Syndrome

In other languages

  • French

  • SRT (Syndrome de Rubinstein-Taybi)
  • Syndrome de Rubinstein et Taybi
  • Syndrome des pouces et des gros orteils trop larges

URI

http://data.loterre.fr/ark:/67375/JVR-WM8ZHH7V-W

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