During the physical exam, your doctor may check for:
- Signs of muscle weakness in your arms, legs, hands and feet
- Decreased muscle bulk in your lower legs, resulting in an inverted champagne bottle appearance
- Reduced reflexes
- Sensory loss in your feet and hands
- Foot deformities, such as high arches or hammertoes
- Other orthopedic problems, such as mild scoliosis or hip dysplasia
Your doctor may also recommend the following tests, which can help provide information about the extent of your nerve damage and what may be causing it.
- Nerve conduction studies. These tests measure the strength and speed of electrical signals transmitted through your nerves. Electrodes on the skin deliver small electric shocks to stimulate the nerve. Delayed or weak responses may indicate a nerve disorder such as Charcot-Marie-Tooth disease.
- Electromyography (EMG). A thin needle electrode is inserted through your skin into the muscle. Electrical activity is measured as you relax and as you gently tighten the muscle. Your doctor may be able to determine the distribution of the disease by testing different muscles.
- Nerve biopsy. A small piece of peripheral nerve is taken from your calf through an incision in your skin. Laboratory analysis of the nerve distinguishes Charcot-Marie-Tooth disease from other nerve disorders.
- Genetic testing. These tests, which can detect the most common genetic defects known to cause Charcot-Marie-Tooth disease, are done by blood sample. Genetic testing may give people with the disorder more information for family planning. Recent advances in genetic testing have made it more affordable and comprehensive. It's important to have genetic counseling before undergoing genetic testing so you know the pros and cons of testing.
There's no cure for Charcot-Marie-Tooth disease. But the disease generally progresses slowly, and it doesn't affect expected life span.
There are some treatments to help you manage Charcot-Marie-Tooth disease.
Charcot-Marie-Tooth disease may sometimes cause pain due to muscle cramps or nerve damage. If pain is an issue for you, prescription pain medication may help control your pain.
- Physical therapy. Physical therapy can help strengthen and stretch your muscles to prevent muscle tightening and loss. A program usually includes low-impact exercises and stretching techniques guided by a trained physical therapist and approved by your doctor. Started early and followed regularly, physical therapy can help prevent disability.
- Occupational therapy. Weakness in the arms and hands can cause difficulty with gripping and finger movements, such as fastening buttons or writing. Occupational therapy can help through the use of assistive devices, such as special rubber grips on doorknobs or clothing with snaps instead of buttons.
Orthopedic devices. Many people with Charcot-Marie-Tooth disease require the help of certain orthopedic devices to maintain everyday mobility and to prevent injury. Leg and ankle braces or splints can provide stability during walking and climbing stairs.
Consider boots or high-top shoes for additional ankle support. Custom-made shoes or shoe inserts may improve your gait. Consider thumb splints if you have hand weakness and difficulty with gripping and holding things.
If foot deformities are severe, corrective foot surgery may help alleviate pain and improve your ability to walk. Surgery can't improve weakness or loss of sensation.
Potential future treatments
Researchers are investigating a number of potential therapies that may one day treat Charcot-Marie-Tooth disease. Potential therapies include medications and in vitro procedures that may help prevent passing the disease to future generations.
Lifestyle and home remedies
Some habits may prevent complications caused by Charcot-Marie-Tooth disease and help you manage its effects.
Started early and followed regularly, at-home activities can provide protection and relief:
- Stretch regularly. Stretching can help improve or maintain the range of motion of your joints and reduce the risk of injury. It's also helpful in improving your flexibility, balance and coordination. If you have Charcot-Marie-Tooth disease, regular stretching can prevent or reduce joint deformities that may result from uneven pulling of muscle on your bones.
- Exercise daily. Regular exercise keeps your bones and muscles strong. Low-impact exercises, such as biking and swimming, are less stressful on fragile muscles and joints. By strengthening your muscles and bones, you can improve your balance and coordination, reducing your risk of falls.
- Improve your stability. Muscle weakness associated with Charcot-Marie-Tooth disease may cause you to be unsteady on your feet, resulting in falls and serious injury. Walking with a cane or a walker can increase your stability. Good lighting at night can help you avoid stumbling and falling.
Foot care is important
Because of foot deformities and loss of sensation, regular foot care is important to help relieve symptoms and to prevent complications:
- Inspect your feet. Check them daily to prevent calluses, ulcers, wounds and infections.
- Take care of your nails. Cut your nails regularly. To avoid ingrown toenails and infections, cut straight across and avoid cutting into the nailbed edges. A podiatrist can trim toenails for you if you have problems with circulation, sensation, and damage to the nerves in your feet. Your podiatrist also may be able to recommend a salon to safely trim your toenails.
- Wear the right shoes. Choose properly fitting, protective shoes. Consider wearing boots or high-top shoes for ankle support. If you have foot deformities, such as a hammertoe, explore having shoes custom made.
Coping and support
Support groups, in conjunction with your doctor's advice, can be valuable in dealing with Charcot-Marie-Tooth disease. Support groups bring together people who are coping with the same kinds of challenges, and offer a setting in which people can share common problems.
Ask your doctor about support groups in your community. The Internet and your local health department, public library and telephone book also may be good sources to find a support group in your area.
Preparing for your appointment
You might first discuss your symptoms with your family doctor, but he or she will probably refer you to a neurologist for further evaluation.
Because there's much to discuss in a short time, try to arrive well-prepared. Here's some information to help you get ready for your appointment and know what to expect from your doctor.
What you can do
- Be aware of any pre-appointment restrictions. At the time you make the appointment, be sure to ask if there's anything you need to do in advance, such as restrict your diet.
- Write down any symptoms you're experiencing, including any that may seem unrelated to the reason for which you scheduled the appointment.
- Make a list of all medications, vitamins or supplements that you're taking.
- Ask a family member or friend to come with you, if possible. Sometimes it can be difficult to remember all of the information provided to you during an appointment. Someone who accompanies you may remember something that you missed or forgot.
- Write down questions to ask your doctor.
Your time with your doctor may be limited, so try to prepare a list of questions. For Charcot-Marie-Tooth disease, some basic questions to ask your doctor include:
- What's the most likely cause of my symptoms?
- What kinds of tests do I need? Do these tests require any special preparation?
- Will this condition go away, or will I always have it?
- What treatments are available, and which do you recommend for me?
- What are the possible side effects for treatment?
- I have other health conditions. How can I best manage these conditions together?
- Do I need to follow any activity restrictions?
- Are there any brochures or other printed material that I can take home with me? What websites do you recommend visiting?
What to expect from your doctor
Your doctor is likely to ask you a number of questions. Being ready to answer them may reserve time to go over any points you want to spend more time on. Your doctor may ask:
- When did you begin experiencing symptoms?
- How severe are your symptoms?
- Do you have symptoms all the time, or do they come and go?
- Does anything seem to make your symptoms better?
- Does anything make your symptoms worse?
- Does anyone in your family have similar symptoms?
- Have you or others in your family had genetic testing to confirm the diagnosis?