AMYOTROPHIC LATERAL SCLEROSIS

AMYOTROPHIC LATERAL SCLEROSIS Amyotrophic lateral sclerosis, also known as ALS, Lou Gehrigs Disease, or Motor Neuron Disease, is a fatal neuromuscular disease that progressively weakens muscles and eventually results in paralysis. It attacks nerve cells in the brain and spinal cord and without messages being sent by the neurons to separate of the brain that control the muscles movement is impossible. Be character muscles argon no longer receiving signals to work, they start to waste away. This is known as atrophy, which makes limbs show up to be thinner.         Symptoms of ALS be similar to many new(prenominal) neuromuscular diseases, making it hard to diagnose quickly. Some symptoms are red ink of muscle control and strength, falling or stumbling, obstacle oratory and breathing, muscle cramps or ticking, and chronic fatigue. With all of these symptoms and the despotic parts of the body that it does affect, ALS does not affect the mind, in the palpate of thoughts, memories, and knowledge.         There are three types of ALS; the most commonality is sporadic, then familial and Guamian. Familial ALS, the hereditary kind, accounts for just 10% of all cases. Of all the familial cases, about 20% are a known ancestral defect. The defect is a sport of superoxide dimutase 1(SOD 1). Because of this percentage, it is obvious that other unidentified genetic cause exist.         ALS is one of the most common neuromuscular diseases worldwide. It affects face pack of both sexes and all races. In the United States, at that luff are 30,000 tidy sum living with the disease. Everyday, 15 more people are diagnosed. Only 50% live longer than 18 months after diagnosis. Another 10% live longer than 10 years. This life expectancy can be greatly plus if the patient decides to go on a ventilator.         ALS patients normally die due to insuffient oxygen that has caused too much carbon... If you! coercion to get a full essay, order it on our website: OrderCustomPaper.com

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