A rare form of axonal peripheral sensorimotor neuropathy with characteristics of classical Charcot-Marie-Tooth type 2 signs and symptoms (progressive weakness and atrophy of distal limb muscles, mild sensory deficits of position, vibration and pain/t
autosomaal dominante hereditaire motorische en sensorische neuropathie type 2 door 'kinesin family member 5A'-mutatie