A rare hereditary motor and sensory neuropathy characterized by intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with usual cl
maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante A
SNOMEDCT-BE (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with usual cl / 765744006
SNOMEDCT-BE (disorder) / 765744006