A form of neuropathy that can begin between childhood and young adulthood; characterized by weakness and atrophy of the muscles of the hands and lower legs; progression is slow and individuals affected can have a normal life span; inheritance is X-linked recessive or X-linked dominant.

synoniem: hereditary motor and sensory neuropathy.

Pools: choroba Charcota-Mariego-Tootha, dziedziczne neuropatie ruchowo-czuciowe