Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain

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Name:
Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain
Description:
A rare subtype of autosomal dominant intermediate Charcot-Marie-Tooth disease characterized by debilitating neuropathic pain associated with mild, distal, symmetrical lower limb sensory loss and mild or absent motor dysfunction. Patients typically manifest with burning, aching, shooting, or throbbing pain and intermittent paraesthesia in toes, heels and ankles.
ORPHAcode:
324585
Synonyms:
Autosomal dominant intermediate CMT disease with neuropathic pain
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Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14