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Rare Neurological Disease Charcot Marie Tooth


Article Written By: taamiv

Charcot Marie Tooth (CMT) is one of the most common neurological diseas, and the most common subtype is the Type 1a. It can be seen in 1 out of every 2500 people. It is no more a rare disease and the number of people suffering from it is increasing day by day.

Generally, Charcot Marie Tooth falls into the category of Muscular Dystrophy family. As the signals from the nerves weaken, the muscles begin to atrophy. Nerves very much resemble the electric wires in general which are used for the passage of electricity. The same is the case with nerves, they provide necessary signals to different muscles of the body but at times these nerves become weak and develop resistance in them for one reason or another.

As the resistance increases the muscles efficiency reduces. This is usually begins with the peripheral limbs (hands or feet). Hands and feet are the first one to suffer from this, however, there assumes to be many more things attach with this disease and it only attacks your limbs but it has impact on your whole body in one way or another. Symptoms can be different in different people. For instance, at age 10 there may be a person on wheel chair while at same age the other person may be running marathon.

The most common symptom of Charcot Marie Tooth is high arches in the feet. These high arches are particularly found in weak muscles and ankles and cause balance problems. The people affected with CMT stumbles a lot along with pain in legs and feet.

In kids these is sometimes misperceived by the parents as growing pain and stumbling. It is not easy to diagnose the symptoms of CMT in the patients until or unless it is diagnosed in his family. CMT cause stumbling, high arches, problem in writing, restless leg syndrome and hammer toes. The other symptoms of CMT involve burning in hands, legs, feet and arms. To conclude we can say that CMT in general sense is a very painful disease that needs immediate treatment once it is diagnosed.


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This Article Has Been Published on Thu, 22 Jul 2010 and Read 230 Times


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