First its sclerosis .. a disease that affects the cells responsible for movement

The first lateral hardening is one of the types of motor neuron disease that affects the neurons in the brain that is responsible for movement over time. The initial lateral sclerosis causes the weakness of voluntary muscles, such as those used to control the legs, arms and tongue, as a person may experience movement problems, such as maintaining balance, slowly moving and wavering, and the injured may eventually experience problems when chewing, swallowing and talking. This rare disease can affect a person of any age, but it usually affects people between 40 and 60 years and is more frequent in men than women. This is usually confused between initial lateral sclerosis and another more common disease than motor neuron diseases, called atrophic lateral sclerosis, and although the initial lateral sclerosis is probably associated with atrophic lateral sclerosis, the initial lateral sclerosis develops at a slower rate of atrophic lateral sclerosis, as it is not dead in most cases. Symptoms usually take the indicators and symptoms of the initial lateral hardening to develop, and generally start in the bones. Among the indicators and symptoms of the disease are the following: Slow movement. Hand trembled. Struggling to chew and swallow. Magia, stumbling and difficult balance. The leg muscles are tense, weak and shrunk. Like the sound, slow speech, overlap and saliva. Repeated, fast and sometimes radical disorder (volatility in the state of mind). In rare cases, breathing problems and bladder in the late stages of the disease. The causes of nerve cells in the brain infected with the movement (upper motor neurons), in the development of the first lateral hardening disease, relax slowly and fail over time. It produces the inability of the nerves to stimulate the motor nerve cells in the spicy cord that controls the muscles. This loss causes movement problems such as the trouble of balance, weakness, slow movement, blowing and pronunciation and swallowing problems. The first sclerosis that begins from adulthood is still the cause of the infection of the first side cllerosis that begins in the unknown childhood, and in most cases it is not classified as a genetic disease, and it is not the cause of its incidence or how to start with infection. Primary lateral jurisprudence occurs in the first cavity of the Als2 Jinn (atrophic lateral hardening 2). Although researchers do not understand how this gene caused the disease, they know that the ALS2 -no instructions to form an alsine protein, which occurs in the cells of the motor neurons. And when the instructions are changed by a person with primary silk hardware disease, the alsine protein becomes unstable and does not work in a right way, which in turn causes an imbalance in the function of the natural muscle. The first lateral lateral hardness is a recessive physical illness, which means that both parents should be pregnant with the gene until the child is inherited, although they do not develop the disease. Complications can be exacerbated by the first average sidewalk for up to 20 years, and its effects vary from person to person. Some may be able to walk, but others will have to use animated chairs or other aid devices. In most cases, it is not believed that the first lateral hardening in adults limits the average life expectancy, but it can gradually affect the quality of life and the number of disabled muscles is increasing. This can cause weak muscles, which can lead to injuries. Chewing and swallowing problems can cause malnutrition. Perhaps it is difficult to put on the performance of daily living activities such as bath and clothing. Medicine -therapy. Physiotherapy and occupational therapy. The treatment of speech and language diseases. Food support. Help devices.