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You are here: Home / Guides / Charcot-Marie-Tooth Disease
Feet of a person with CMT

Charcot-Marie-Tooth Disease

01/05/2023

Charcot-Marie-Tooth disease, also known as CMT, is a hereditary condition that affects the peripheral nerves, causing weakness and wasting of the muscles in the legs, arms, and hands. This disease affects approximately 1 in 2,500 people worldwide and is the most common inherited disorder of the peripheral nervous system. At Mobility Centre, we believe it’s essential to raise awareness of CMT to promote early diagnosis and access to the right aids that can help individuals live their lives to the fullest. 

What is Charcot-Marie-Tooth disease? 

Charcot-Marie-Tooth disease is caused by mutations in genes that affect the structure and function of peripheral nerves. These nerves are responsible for transmitting signals from the brain and spinal cord to the rest of the body, allowing us to move our limbs and feel sensations. In people with CMT, the peripheral nerves are progressively damaged, leading to muscle weakness, decreased sensation, and loss of coordination. 

Symptoms of Charcot-Marie-Tooth disease 

The symptoms of Charcot-Marie-Tooth disease can vary widely depending on the type of mutation and the severity of the disease. Typically, the earliest signs are noticed during childhood or adolescence and include: 

  • Weakness in the legs, feet, and ankles 
  • Frequent tripping or falling 
  • Difficulty with tasks that require fine motor skills, such as buttoning clothes or writing 
  • Decreased sensation in the hands and feet 
  • High arches or flat feet 
  • Clawed toes or fingers. 

As the disease progresses, muscle weakness and atrophy can spread to the arms, hands, and shoulders, making it difficult to perform everyday tasks. Some people with CMT may also experience chronic pain, fatigue, and difficulty with balance. 

Treatment and Management of Charcot-Marie-Tooth disease 

There is currently no cure for Charcot-Marie-Tooth disease, but there are several treatment options that can help manage symptoms and improve quality of life. These include: 

Physical therapy: Physical therapy can help maintain muscle strength, improve balance, and prevent contractures. 

Occupational therapy: Occupational therapy can help individuals with CMT learn new techniques and strategies to perform daily activities and work-related tasks. 

Orthotics: Wearing braces or orthopaedic shoes can help support weak muscles and prevent foot deformities. 

Surgery: In severe cases, surgery may be necessary to correct deformities or release compressed nerves. 

Medication: There is currently no medication specifically approved for treating Charcot-Marie-Tooth disease, but some drugs may help manage symptoms such as pain or muscle spasms. 

Living with Charcot-Marie-Tooth disease 

Living with Charcot-Marie-Tooth disease can be challenging, but with the right support and resources, individuals with CMT can live full and productive lives. Some tips for managing CMT include: 

Staying physically active: Regular exercise, such as walking or swimming, can help maintain muscle strength and flexibility. 

Eating a healthy diet: A balanced diet can help support overall health and reduce the risk of other health problems. 

Seeking emotional support: Coping with a chronic illness can be stressful, so it’s essential to seek support from friends, family, or a mental health professional. 

Using assistive devices: Tools such as canes, walkers, or mobility scooters can help individuals with CMT stay independent and active. 

Charcot-Marie-Tooth disease is a hereditary condition that affects the peripheral nerves, causing muscle weakness and wasting. While there is no cure for CMT, there are several treatment options that can help manage symptoms and improve quality of life. By raising awareness of this condition, we hope to promote early diagnosis and access to the right products that can help individuals with CMT live their lives to the fullest. 

More Information & Support 

Charcot-Marie-Tooth disease (CMT) | Health Navigator NZ 

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