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Charcot-Marie-Tooth disease axonal type 2L

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Description

A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy. In the single family reported to date, CMT2L onset is between 15 and 33 years. Patients present with a symmetric distal weakness of legs and occasionally of the hands, absent or reduced tendon reflexes, distal legs sensory loss and frequently a pes cavus. Progression is slow.

ORDO

  • Mode of Inheritance

  • Autosomal dominant inheritance
  • Heterogeneous

VARIANTS

85

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Genes

External Links

  • OMIM

    608673

  • Orphanet

    99945

  • HPO
  • Medgen

    C1837552

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