It is our first instinct to think that this illness is related to either a woman named Mary or a tooth for the sake of name, but it is not the case. Yes, this disease has an interesting name, but it is not fun for those who have it. Because Charcot-Marie Tooth disease (aka CMT) is the most common inherited neuropathy, there is a common point that one out of 2,500 Americans suffers. It is a hereditary disorder, but it can also be caused by spontaneous mutations. Professor Jean Martin Charcot and his student Pierre Marie pointed out that the disease is the fibula (nerve of the limb), muscle atrophy (waste of the body part). Exactly the same year Howard Henry Tooth explained this disease as peritoneal progressive muscular atrophy. He was not the problem of spinal cord or bone marrow but the first time to correctly symptom the neurological problem. As the year goes on, we have learned more about the disease, but there is no cure yet. We have found more ways to respond to the symptoms of CMT.
CMT has several different types.
CMT1 is a disease affecting the gene that makes myelin protein in the foot. Myelin is a protective barrier on the axon and is the part of the nerve that sends information to the rest of the body. The myelin sheath made in CMT patients is easily broken down, the work speed of the feet slows and the hands hurt. This leads to weakness and paralysis of these spinal columns.
CMT 2 is an axon neuropathy. In this modified example, peroneal muscle atrophy occurs because the axon of the foot dies. Warrior degeneration can also occur.
CMT 3 is characterized by an early childhood on the set. Most CMT patients show symptoms during the first 20 years, but the infant's sunset appears in the first two years of life. This change is very tough. It is also characterized by partial demi-miniton as well as myelin thinning.
CMTX, also known as CMT4, is retained on the X chromosome. This mutation is also characterized by demyelination of neuropathy.
CMT occurs first in lower limbs. This can create a lack of desire for causing clumsiness or being active. A serious symptom of this disease is severe muscle degeneration. Due to the lack of neurotransmission between the brain and the feet, various foot deformations can occur. When you drop your feet, you need to pick up your feet to lower your feet from the ground. It is also very common, not only with hammer and pes cabbas (high arches).
There is no cure for CMT yet, but there are several different ways to help alleviate degeneration, as well as relieving the pain caused by foot deformity. Physical therapy and strength training are two very useful treatments for CMT patients. Shoes with good support for the metatarsal and ankle, surgery on the soles of the feet, stretching, and painkillers are also valuable methods to support CMT.
If you know that no one has CMT, pay a little bit of attention today ... This is not a simple illness. If you think that you or someone you know is suffering from Charcot-Marie-Tooth sickness, please go to Podiatrist. There are methods and test methods to deal with symptoms related to this disease.
