(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)
choroba Charcota-Mariego-Tootha, dziedziczne neuropatie ruchowo-czuciowe
synonim: hereditary motor and sensory neuropathy