ALS . (1969, December 31). In MegaEssays.com. Retrieved 20:24, October 09, 2018, from https://www.megaessays.com/viewpaper/58922.html

My medical history is full of diseases and diseases, from a cold to a deadly murderer. Some may be easy to treat, some may be the end of life, but some of the worst is yet to be cured, and one such disorder is amyotrophic lateral sclerosis .

Amyotrophic lateral sclerosis (ALS) is a degenerative disease that affects the human nervous system. This is a fatal disease that kills and kills the victim because the body's motor neurons are destroyed. Motor neurons are brainstem and spinal cord neurons that control muscle contraction. In ALS, these neurons deteriorate to the point where all movement including breath ceases. Muscle weakness first occurs in muscles (such as hands) that are separate from parts of the brain's body, then spreads to other muscle groups close to the brain. However, this early symptom is hard to notice

Early symptoms of amyotrophic lateral sclerosis are very mild and tend to be overlooked. They begin with simple things, such as stumble and dropping things. Cramps and cramps in the muscles, and abnormal fatigue of the arms and legs occur soon and may cause difficulties in daily activities such as walking and dressing. However, at a later stage, shortness of breath or difficulty in breathing or swallowing becomes difficult until the body is completely infected with the disease. Intelligence, eye movement, bladder function and sensation are the only ability to escape.

The origin and location of this deadly disease has not been clarified, but it was originally decided by famous French neurologist Jean-Martin Chakcott in 1869. Amyotrophic lateral sclerosis is not contagious, but the cause of the disease remains ambiguous. Currently, ALS has three recognized forms. Genetic, interspersed, and guamanian. The genotype of ALS seems inherited or inherited in the family, and about 10% of ALS patients have a family history of the disease. one

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