Abstract
The Charcot-Marie-Tooth disease, also known as hereditary motor and sensory neuropathy (HMSN) is a clinically and genetically heterogeneous group of diseases that affect the sensory and motor nerves of the peripheral nervous system (PNS). They can be classified according to motor nerve conduction velocities into CMT1 (demyelinating subtypes), CMT2 (axonal subtypes) and CMTi (intermediate …