Autosomal dominant Charcot-Marie-Tooth disease type 2D

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Name:
Autosomal dominant Charcot-Marie-Tooth disease type 2D
Description:
A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterized by distal weakness primarily and predominantly occurring in the upper limbs and tendon reflexes absent or reduced in the arms and decreased in the legs. Progression is slow.
ORPHAcode:
99938
Synonyms:
CMT2D
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14