Charcot-Marie-Tooth disease - an inherited neurological disorder | Children's Charity

Charcot-Marie-Tooth disease - an inherited neurological disorder

Published on 30 May 2017

Estimates suggest around 25,000 people in the UK have Charcot-Marie-Tooth disease (CMT).1 They usually start to have symptoms – which can include muscle weakness and numbness in the feet, arms and hands – during childhood or adolescence. Symptoms slowly get worse and more disabling over time, making everyday tasks increasingly difficult. Professor David Bennett, of the University of Oxford, is in the early stages of developing a new treatment – a gene therapy – for children with CMT. There’s no cure for CMT, and no way to slow down the progression of the disease, so improvements in treatment are badly needed.

How are children’s lives affected now?

People with CMT, an inherited condition, usually experience their first symptoms when they’re between five and 15 years old.

Symptoms vary from one child to another. Early signs of CMT in a young child can be difficult to spot. A child might just seem clumsy or accident prone, for example, or they might find it difficult to walk, because of problems lifting their feet off the ground. As the children can have high insteps, it may be difficult to get shoes to fit.

Symptoms get worse and more disabling over time, although CMT is unpredictable, so it’s not possible to tell how quickly this will happen or how severe symptoms will become.

Symptoms that can get worse include muscle weakness and some loss of feeling in the hands and arms, which make everyday tasks such as writing, doing up buttons or opening jars difficult. Children can also have problems with walking and with posture, which can put excessive strain on the body and cause debilitating pain.

How could this research help?

“Our ultimate goal is to develop new treatments for CMT,” says Professor Bennett. “At the moment, we are focusing on the most common form of CMT, called CMT1A.”

The symptoms of CMT1A result from damage to peripheral nerves, which are found outside of the brain and spinal cord. A substance called myelin, which normally forms a protective coating around nerves, is damaged, as children with the condition have an excess dosage of the gene called PMP22, which makes myelin unstable.

The team aims to develop a new treatment – a form of gene therapy – that stops, slows down or even repairs this damage to myelin. They are investigating a possible way to do this in the laboratory. “Our approach involves helping cells to produce a protein called neuregulin 1, or NRG1, which plays a pivotal role in controlling the production of myelin,” says Professor Bennett. “The aim of this project is to see if this protein can help myelination of cells derived from patients with CMT1A.”

This work is in its early stages, but a new treatment that prevents or slows down disease progression, and stops children’s symptoms from getting worse, would be a major step forward.

References

1. CMT UK. http://cmt.org.uk/about-cmt/what-is-cmt/ Website accessed 15 January 2017.

 

Project LeaderProfessor David L H Bennett MB PhD FRCP
Project team
  • Dr Ilaria Cervellini PhD
LocationNuffield Department of Clinical Neurosciences, John Radcliffe Hospital, University of Oxford
Duration3 years
Grant awarded21 November 2017
Start date1 January 2017
End date31 December 2019
Grant amount£199,918.00
Grant codeGN2526

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