The classification of Charcot-Marie-Tooth diseases, a never-ending story: CMT4?

Author:

Vallat Jean-Michel12,Tazir Meriem3,Magy Laurent12,Le Masson Gwendal45,Mathis Stéphane45

Affiliation:

1. Department of Neurology, University Hospital Dupuytren, 2 avenue Martin Luther King, 87042 Limoges, France

2. National reference center ‘neuropathies périphériques rares’, University Hospital Dupuytren, 2 avenue Martin Luther King, 87042 Limoges, France

3. Department of Neurology, University Hospital Mustapha Bacha, Algiers, Algeria

4. Department of Neurology, Nerve-Muscle Unit, CHU Bordeaux (Pellegrin University Hospital), University of Bordeaux, Place Amélie Raba-Léon, 33000 Bordeaux, France

5. National reference center ‘maladies neuromusculaires du grand sud-ouest’, CHU Bordeaux (Pellegrin University Hospital), University of Bordeaux, Place Amélie Raba-Léon, 33000 Bordeaux, France

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Reference10 articles.

1. Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q;Ben Othmane;Hum Mol Genet,1993

2. SURF1 deficiency causes demyelinating Charcot-Marie-Tooth disease;Echaniz-Laguna;Neurology,2013

3. Updating the classification of inherited neuropathies: results of an international survey;Magy;Neurology,2018

4. Charcot-Marie-Tooth diseases: an update and some new proposals for the classification;Mathis;J Med Genet,2015

5. Reasons Charcot-Marie-Tooth disease due to mutations in the MME gene should not be named AR-CMT2T;Mathis;Ann Neurol,2016

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