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Concept information

Terme préférentiel

Charcot-Marie-Tooth Disease  

Type

  • mesh:Descriptor

Définition

  • A hereditary motor and sensory neuropathy transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and loss of reflexes in the muscles of the legs (and occasionally involving the arms). Onset is usually in the second to fourth decade of life. This condition has been divided into two subtypes, hereditary motor and sensory neuropathy (HMSN) types I and II. HMSN I is associated with abnormal nerve conduction velocities and nerve hypertrophy, features not seen in HMSN II. (Adams et al., Principles of Neurology, 6th ed, p1343)

Synonyme(s)

  • Atrophy, Muscular, Peroneal
  • Charcot-Marie Disease
  • Charcot-Marie-Tooth Hereditary Neuropathy
  • Charcot-Marie-Tooth Syndrome
  • Muscular Atrophy, Peroneal
  • Peroneal Muscular Atrophy

Traductions

  • français

  • Amyotrophie de Charcot-Marie-Tooth
  • Amyotrophie péronière
  • Atrophie musculaire péronière
  • Maladie de Charcot-Marie

URI

http://data.loterre.fr/ark:/67375/JVR-HJN06C33-8

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RDF/XML TURTLE JSON-LD Date de création 08/11/1999, dernière modification le 08/07/2013