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Charcot-Marie-Tooth disease type 2E

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Description

A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, with onset in the first to 6th decade with a gait anomaly and a leg weakness that reaches the arms secondarily. Tendon reflexes are reduced or absent and, after years, all patients have a pes cavus. Other signs may be present, including hearing loss and postural tremor.

ORDO

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

166

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Genes

External Links

  • OMIM

    607684

  • Orphanet

    99939

  • HPO
  • Medgen

    C1843225

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