Autosomal dominant Charcot-Marie-Tooth disease type 2Q

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Name:
Autosomal dominant Charcot-Marie-Tooth disease type 2Q
Description:
A rare subtype of autosomal dominant Charcot-Marie-Tooth disease type 2, characterized by adolescent to adulthood-onset of symmetrical, slowly progressive distal muscle weakness and atrophy (with a predominant weakness of the distal lower limbs) associated with reduced or absent deep tendon reflexes, pes cavus and mild to moderated deep sensory impairment.
ORPHAcode:
329258
Synonyms:
CMT2Q
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14