Autosomal dominant Charcot-Marie-Tooth disease type 2V

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Name:
Autosomal dominant Charcot-Marie-Tooth disease type 2V
Description:
A rare, axonal hereditary motor and sensory neuropathy characterized by adult onset of recurrent pain in legs with or without cramps, progressive loss of deep tendon reflexes and vibration sense, paresthesias in the feet and later in the hands. Patients often experience sleep disturbances and mild sensory ataxia.
ORPHAcode:
447964
Synonyms:
Autosomal dominant Charcot-Marie-Tooth disease type 2 due to NAGLU mutation
CMT2V
Hereditary adult-onset painful axonal polyneuropathy
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Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14