Side -muscle click: Learn the most prominent information

Amyotrophic laterral sclerosis under the protection of the atrophic sclerosis of the side muscle is the most common disease among the diseases that belong to the peripheral hypothesis, where this disease is gradually damaged by the motor nerves in the brain and spinal cord, and this disease is characterized by a continuous decrease in motor ability until it reaches a state of muscle. The disease occurs mainly in ages between 50 and 70 and occurs a little more frequently in men against women. Symptoms of lateral muscle sclerosis include symptoms as follows: Problems for walking or doing normal daily activities. Tension and fall. Weakness in your leg, feet or ankles. Hand weakness. Interfere in speech or problems with swallowing. Muscle cramps and tremors in your arms, shoulders and tongue. Cry, laugh or yawn. Cognitive and behavioral changes. Causes and factors of the risk of lateral muscle sclerosis include causes and risk factors the following: 1. Genetics The 5% – 10% of people with atrophic lateral sclerosis inherit it, as their children with most people with atrophic lateral sclerosis of the family have an opportunity to develop the disease. 2. Age increases the risk of infection with atrophic lateral sclerosis with age, which occurs more frequently between the ages of the 1940s and middle fifths. 3. Sex before the age of 65 has men a little more atrophic sclerosis. 4. Smoke smoke is the only environmental risk factor for atrophic lateral sclerosis, as it appears that the risk is greater for women, especially after menopause. 5.. Exposure to toxins in the environment. Some evidence suggests that exposure to bullets or other materials in the workplace or at home can be linked to atrophic side cllerosis. Complications of lateral muscle sclerosis include the most important complications as follows: 1. Breathing problems over time paralyze its muscles of the sclerosis you use to breathe as you need an apparatus to help you breathe at night. 2.. Talking problems Most people with atrophic lateral sclerosis suffer from trouble talking as it usually starts in the form of a slight overlap in words, but it gets worse. The speech eventually becomes difficult for others to understand, and people with atrophic side cllerosis are often dependent on other communication techniques to communicate. 3. Eating problems can develop people with atrophic lateral sclerosis with malnutrition and dehydration due to muscle damage that controls swallowing. It is also more likely to enter food, fluid or saliva in the lungs, which can cause pneumonia. 4. Dementia, some people with atrophic lateral sclerosis suffer from memory and decision -making problems, and some are eventually diagnosed as a form of dementia called temporal frontal dementia. Diagnosis of lateral muscle sclerosis is difficult to diagnose the atrophic lateral sclerosis, because it can simulate other neurological diseases, tests to exclude other conditions may include: 1. The muscle -electric scheme that puts your doctor an electrode needle over your skin in different muscles and the test assesses the electrical activity of your muscles. Misroses of the muscles found in the electrocardiogram can help doctors diagnose or exclude atrophic side cllerosis, as the muscle electric scheme can also help guide your athletic treatment. 2. The study of nervous conductivity. 3. MRI using radio waves and a strong magnetic field. MRI is detailed images of the brain and spinal cord, where magnetic resonance imaging can reveal spinal cord tumors, open tablets in your neck or other cases that can cause your symptoms. 4. Blood and urinary analyzes can help your doctor’s blood and urinary samples get rid of other possible causes of signs and symptoms. 5. The cotton puncture. This includes the removal of a sample of the pipeline fluid for laboratory examination with a small needle placed between two paragraphs at the bottom of your back. Side -muscle glerosis -Therapy contains the most important treatments the following: 1. Drug therapy includes the following: Riluzole. If this remedy is taken orally, it has been proven to increase average life expectancy by three to six months, but it can cause side effects, such as dizziness, digestive diseases and liver function changes. Edaravone has shown that this drug given in the vein reduces the decline of daily performance, as its life effect is still unknown, and side effects may include bruising, headaches and shortness of breath. 2. Other treatments include treatments as follows: Breathing care will eventually face more breath as your muscles weaken, so doctors can experience your breathing regularly and provide your devices to help breathe at night. Physiotherapy can treat pain, walking, mobility, reinforcement and equipment needs that help you stay independent. Regular exercise can also help improve your sense of well -being, and appropriate stretching can help prevent pain and help your muscles work at best. The practice of practice can help the professional therapist find ways to stay independent, despite the weakness of the hand and the arm, as adaptable equipment can help you carry out activities such as wearing clothing, personal care, eating and bathing. Speech therapy can teach you adaptable techniques to make your words more understandable, as the speech therapist can also help you explore other ways to communicate, such as the alphabet or pen and paper. Food support Your team will work with you and your family members to ensure that you eat food that is easy to swallow and meet your nutritional needs, and you may eventually need a diet. Psychological and social support. Your team may include a social worker to help with financial problems, obtain insurance, equipment and pay the price of the devices you need. Psychologists, social workers and others can provide you and your family with emotional support. The prevention of atrophic sclerosis of the side cannot be prevented by the disease.