Late onset Charcot–Marie–Tooth 2 syndrome caused by two novel mutations in the MPZ gene

Abstract

MPZ gene mutations cause demyelinating and axonal Charcot–Marie–Tooth (CMT) disease. Two novel MPZ mutations are reported in very late onset and progressive CMT syndrome. The N60H caused axonal CMT in a large family, whereas the I62M occurred in a single patient presenting with a primary axonal neuropathy. Previously, chronic polyradiculoneuritis was assumed in two patients. Molecular genetic testing and particularly screening for MPZ mutations in late onset neuropathies are important to differentiate acquired and inherited neuropathies.