Autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation

Orpha code: 435819OMIM code:

Definition

A rare, axonal hereditary motor and sensory neuropathy characterized by adult onset of slowly progressive distal muscle weakness and atrophy, decreased deep tendon reflexes of lower limbs, and mild distal sensory loss leading to gait difficulties in most patients.

Disease data
Classification

Disease

Synonyms
CMT2 due to TFG mutation
CMT2 spowodowana mutacją TFG
ORPHA code
435819
OMIM code
-
ICD10 code
G60.0
ICD11 code
-

No additional description.

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