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Charcot-Marie-Tooth disease

Background

Charcot-Marie-Tooth disease: CMT: Peroneal Muscular Atrophy: Hereditary Motor and Sensory Neuropathy

This is a genetic disorder characterised by slowly progressive muscular weakness.

The onset of the condition may be from childhood to late middle or old age.

What are the symptoms? View What are the symptoms?

Medical text written November 1991 by Contact a Family. Approved November 1991 by Professor M Patton, Professor of Medical Genetics, St Georges Hospital Medical School, London, UK and Dr J E Wraith, Consultant Paediatrician, Royal Manchester Children's Hospital, Manchester, UK. Last updated August 1999 by Dr David Hilton-Jones. Last reviewed January 2004 by Dr David Hilton-Jones, Clinical Director, Muscle and Nerve Centre, Radcliffe Infirmary, Oxford, UK.

 

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