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Charcot-Marie-Tooth Disease: A Neurological Disorder

By HERWriter
 
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Charcot-Marie-Tooth disease is not, as it may appear at first glance, a problem to take to your dentist. It is actually an inherited neurological disorder whose unusual name comes from the two French neurologists, Jean Charcot and Pierre Marie, and the English doctor Howard Henry Tooth, who clinically described it in 1886.

Other names for this condition are Charcot-Marie-Tooth hereditary neuropathy, Charcot-Marie-Tooth syndrome, hereditary motor and sensory neuropathy (HNSN), and Peroneal Muscular Atrophy (PMA).

Charcot-Marie-Tooth disease (CMT) involves muscle weakness and loss of sensation, predominantly in the arms and legs, especially in the calves.

This disease affects the periphery nerves, which control muscles and send messages from the legs and arms to the brain. These messages give us our sense of touch.

The disorder generally makes itself known in childhood or adolescence, though this can happen at any age.

The earliest indicators of CMT are usually clumsiness and weakness in the ankles, feet and legs. The feet may be either extremely arched or extremely flat, and the toes may be curled upwards, into "hammertoes".

Walking is awkward due to weak ankle muscles which causes the individual to step higher than normal, or the toes may drop forward.

Arms and feet become numb. Injuries can occur due to lack of sensation. The lower legs are quite thin, and have been described as "stork legs".

Cramping can occur in the lower legs and forearms, and some of the body's reflexes deteriorate. The hands suffer weakness and atrophy in the muscles, and fine motor ability decreases.

Balance becomes precarious. The spine may curve (scoliosis). There may be some hearing or sight loss.

Symptoms vary widely from individual to individual. Some people will have mild symptoms that do not interfere with their ability to live normal lives. Very often though, numbness and weakness will have far-reaching effects.

While CMT does not affect life expectancy, there is no cure. But treatments are available that can make a difference in quality of life.

Physical therapy can stretch and strengthen the weak muscles. Occupational therapy will help the individual learn new ways to better handle the challenges of daily life.

Orthopedic devices, like braces or splints, or special shoes or inserts, can help the individual to walk more easily.

Thumb splints can cause a return of some dexterity. A back brace may be in order for those with scoliosis. In cases of severe deformity, surgery may be performed.

Resources

Learning About Charcot-Marie-Tooth Disease
http://www.genome.gov/11009201

Genetics Home Reference: Charcot-Marie-Tooth disease
http://ghr.nlm.nih.gov/condition=charcotmarietoothdisease

Charcot-Marie-Tooth Disease
http://emedicine.medscape.com/article/315260-overview

What Is Charcot-Marie-Tooth Disease (CMT)? What Causes Charcot-Marie-Tooth Disease?
http://www.medicalnewstoday.com/articles/172056.php

Charcot-Marie-Tooth Disease Fact Sheet
http://www.ninds.nih.gov/disorders/charcot_marie_tooth/detail_charcot_marie_tooth.htm

Mayo Clinic: Charcot-Marie-Tooth disease
http://www.mayoclinic.com/health/charcot-marie-tooth-disease/DS00557

Visit Jody's website and blog at http://www.ncubator.ca and http://ncubator.ca/blogger

Add a Comment2 Comments

HERWriter

That diagnosis must have come as a shock. Or then again, maybe not.

As you say, it explained alot. So maybe you'd been living with unanswered questions all this time.

Not an easy disease to live with. It imposes many limitations and complications for you to have to deal with in your day to day life.

I admire your conscious decision to persevere and overcome. Hang onto that hope and determination. I wish you great success.

February 13, 2010 - 9:55pm
EmpowHER Guest
Anonymous

I was just diagnosed with Charcot-Maire-Tooth... it explains a lot about my inability to keep up with my peers when I was younger (in terms of running).

Further, I have developed osteoarthritis at the ripe old age of 30 because of the weight compensation required to walk normally, given my calf muscles are so extremely atrophied.

This disease, like so many other forms of muscular dystrophy provide people with two choices: 1) overcome or 2) succumb.

I choose to overcome.

February 12, 2010 - 8:20pm
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We value and respect our HERWriters' experiences, but everyone is different. Many of our writers are speaking from personal experience, and what's worked for them may not work for you. Their articles are not a substitute for medical advice, although we hope you can gain knowledge from their insight.

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