Autosomal dominant Charcot-Marie-Tooth disease type 2I

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Name:
Autosomal dominant Charcot-Marie-Tooth disease type 2I
Description:
A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, characterized by a late onset with severe sensory loss (paresthesia and hypoesthesia) associated with distal weakness, mainly of the legs, and absent or reduced deep tendon reflexes.
ORPHAcode:
99942
Synonyms:
CMT2I
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14