Charcot-Marie-Tooth disease type 2T

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Name:
Charcot-Marie-Tooth disease type 2T
Description:
A rare autosomal recessive axonal hereditary motor and sensory neuropathy characterized by adult onset of slowly progressive distal muscle weakness and atrophy, sensory impairment, and decreased or absent deep tendon reflexes predominantly in the lower extremities. Patients present gait disturbances but remain ambulatory. Mild involvement of the upper limbs may be seen.
ORPHAcode:
495274
Synonyms:
AR-CMT2T
Autosomal recessive axonal Charcot-Marie-Tooth disease type 2T
CMT2T
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Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14