Hereditary motor and sensory neuropathy VIAĬharcot-Marie-Tooth disease, dominant intermediate CĬharcot-Marie-Tooth disease, axonal, type 2DDĬharcot-Marie-Tooth disease, axonal, type 2FFĬharcot-Marie-Tooth disease, dominant intermediate DĬharcot-Marie-Tooth disease, axonal, type 2EEĬharcot-Marie-Tooth disease, axonal, type 2TĬharcot-Marie-Tooth disease, dominant intermediate FĬharcot-Marie-Tooth disease, axonal, type 2WĬharcot-Marie-Tooth disease, demyelinating, type 1JĬharcot-Marie-Tooth disease, axonal, type 2FĬharcot-Marie-Tooth disease, dominant intermediate GĬharcot-Marie-Tooth disease, axonal, type 2H Normal motor nerve conduction velocities Ĭharcot-Marie-Tooth disease, recessive intermediate CĬharcot-Marie-Tooth disease, axonal, type 2A2BĬharcot-Marie-Tooth disease, axonal, type 2A2A Thenar muscle atrophy įirst dorsal interossei muscle weakness įirst dorsal interossei muscle atrophy Ĭold-induced hand cramps īalance impairment Upper limb weakness and atrophy predominates
Distal limb muscle weakness due to peripheral neuropathy ĭistal limb muscle atrophy due to peripheral neuropathy
