Sports neuron disease is a conductive disease, but different types of patients have different diseases, even if the progress of the same type of patient is also different. The average course of myocytreatry side Sidaloids is about 3 years. It can die within 1 year after progress, and the slow disease progresses is sometimes more than 10 years.
Adult spine muscle atrophy is generally developed slowly, the disease is often more than 10 years. Primary lateral sclerosis is rare, generally slowly developed. Death is due to ball paralysis, respiratory muscle paralysis, combined with pulmonary infection or system failure.
Since the causes and pathogenesis of this disease has no exact understanding, there is no effective preventive measures.
In fact, clinical motion neuronal disease is mainly the performance of myocytreatry, and other types of most are different periods of the development of diseases, and the performance of motion system damage is performed, and the ethical contrasts and primary side rings. The hard syndrome ultimately develops the muscles atrophy lateral beambridosis. Sports neurogenesis in simple spinal cord is generally survived by 3-5 years, while the patients with marrow damage (simple or mixed spinal damage) survived less than 2 years and a half, the disease progresses slowly, there are authors reported 10 -15 survival cases . Differentiated patient dysfunction has significant differences in patient dysfunction, and patients in patients with extension damage are complete (about months), while spinal cord damage is slow, up to 4 years. Children can survive 20-40 years.
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