Genetic neuropathy .. causes, symptoms and treatment methods

“Shared Mary Tott” is a group of genetic disorders that cause nerve damage, as this damage is often caused by arms and legs (peripheral nerves), and also called genetic neuropathy in motor and sensory nerves. The disease causes small muscles, and the patient may experience a loss of sensation, muscle cramps and problems. Some of the common problems associated with this disease are the malformations of the foot, such as hammer tones and the height of the bow, usually the symptoms start with the feet and bones, but its effect can eventually reach the hands and arms. Symptoms usually occur in adolescence or early adulthood, but they can also occur in the middle age. Symptoms of neuropathy high brackets. Weakness in the legs, ankles and feet. The muscle mass loss in the legs and feet. Parcel finger (hammer tone). Reduce the ability to run. Trouble to lift the ankle (hang). Walk with disturbance or abnormal mode. Stumbles or falls regularly. Lack of feeling or losing it in the legs and feet. The reasons for neuropathy, “Shareo Mary Tott” are a genetic genetic state and are caused by the presence of mutations in the genes affecting the nerves of the feet, legs, hands and arms. Sometimes these mutations are damaged, and these mutations can affect the protective layer that surrounds the nerve (mile). Both cause poor messages that are transmitted between the parties and the brain. Complications vary complications of the disease in their intensity from person to person, usually feet and problems with the most dangerous problems, and muscles can also be weakened, and some parts of the body affected by the weakness of the sensation are exposed to injuries. Sometimes the muscles of the feet cannot receive brain signals, it can cause it to stumble and fall, and the brain may not receive messages with feet pain, so if the injured place a rubber valve around his finger, he can, for example, develop an infection without feeling. The patient may have trouble breathing, swallowing or talking if the muscles that control these functions are influenced by the disease from shared Marie to. Diagnosis of neuropathy studies of nerve delivery measures these tests strength and speed of electrical signals transmitted by nerves. A muscle -electric scheme places an electric electrode with a thin needle through the skin in the muscles, then the electrical activity is measured during the muscle relaxation and gently tied it. A biopsy of nerves is taken a small piece of peripheral nerve out of the hard leg by making an incision in the skin. Genetics test these tests using a blood sample, which can detect the most common genetic defects known to cause Shareo Mary to. Treatment of neuropathy. There is no treatment for the Charm Mary Tott, but the disease slowly develops in general and does not affect the expected age, but some procedures may be helpful in relieving pain. Physiotherapy can help strengthen the muscles and expand them to prevent muscle tension and loss. Career therapy can lead to weakness in the arms and hands to problems with constipation and fingers. You can therefore benefit from professional therapy using aid devices such as special rubber -hardness on the door handles, or use clothing buttons in clothing instead of normal buttons. Orthopedic devices, many people with the infection of Charm Mary Tots should help bone evaluation devices maintain daily movement and prevent infection. Surgery, if the foot disorders are severe, can help correctional foot surgery to relieve pain and improve the ability to walk, but surgery cannot reduce the weakness or loss of sensation. Possible future treatments see researchers in a number of possible treatments that can one day be treated as a diseases from the Carko Mary. Possible treatments are used by medication, genetic therapy and laboratory procedures that can help prevent the transmission of the disease to future generations.