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Concept information

Preferred term

Ataxia Telangiectasia  

Type

  • mesh:Descriptor

Definition

  • An autosomal recessive inherited disorder characterized by choreoathetosis beginning in childhood, progressive CEREBELLAR ATAXIA; TELANGIECTASIS of CONJUNCTIVA and SKIN; DYSARTHRIA; B- and T-cell immunodeficiency, and RADIOSENSITIVITY to IONIZING RADIATION. Affected individuals are prone to recurrent sinobronchopulmonary infections, lymphoreticular neoplasms, and other malignancies. Serum ALPHA-FETOPROTEINS are usually elevated. (Menkes, Textbook of Child Neurology, 5th ed, p688) The gene for this disorder (ATM) encodes a cell cycle checkpoint protein kinase and has been mapped to chromosome 11 (11q22-q23).

Entry terms

  • Ataxia-Telangiectasia
  • Ataxia Telangiectasia Syndrome
  • Louis-Bar Syndrome
  • Telangiectasia, Cerebello-Oculocutaneous

In other languages

  • French

  • AT (Ataxie-Télangiectasie)
  • Ataxie télangiectasique
  • Ataxie-télangiectasies
  • Syndrome d'ataxie-télangiectasie
  • Syndrome de Louis-Bar

URI

http://data.loterre.fr/ark:/67375/JVR-DP8WB99S-5

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