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Updated: May 31, 2026

Modeling Charcot-Marie-Tooth Disease In Vitro by Transfecting Mouse Primary Motoneurons
Published on: January 7, 2019
Mitochondrial disease mimicking Charcot-Marie Tooth disease
M Needham1, J Duley, S Hammond
1Department of Neurology, Royal North Shore Hospital and University of Sydney, Sydney, New South Wales, Australia.
Abstract:
Charcot-Marie tooth disease (CMT) is a heterogenous group of peripheral neuropathies caused by various genetic defects. Three cases of mitochondrial myopathy, neuropathy and gastrointestinal encephalopathy (MNGIE) which initially presented with a peripheral neuropathy resembling CMT are described here. The diagnosis in all three cases was made after they developed eye signs and abdominal complaints. Young patients with mutation negative CMT should be followed up to monitor for signs of MNGIE.
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