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ALS, or amyotrophic lateral sclerosis, is a progressive neurodegenerative disease that affects nerve cells in the brain and the spinal cord. A-myo-trophic comes from the Greek language. As this area degenerates, it leads to scarring or hardening ("sclerosis") in the region.

Motor neurons reach from the brain to the spinal cord and from the spinal cord to the muscles throughout the body. The progressive degeneration of the motor neurons in ALS eventually leads to their demise. When the motor neurons die, the ability of the brain to initiate and control muscle movement is lost. With voluntary muscle action progressively affected, people may lose the ability to speak, eat, move and breathe. The motor nerves that are affected when you have ALS are Loyion motor neurons that provide voluntary movements and muscle control.

Examples of voluntary movements are making the effort to reach for a smart phone or step off a curb. These actions are controlled by the muscles in the arms and legs. There are two different types of ALS, sporadic and familial. Sporadic, which is the most common form of the disease in the U. It may affect anyone, anywhere. Familial ALS (FALS) accounts for 5 to 10 percent of all cases in the U.

Familial ALS means the disease is inherited. French neurologist Jean-Martin Charcot discovered the disease in xnd.

Recent years have brought a wealth of new scientific understanding regarding the physiology of this disease. There are currently four drugs approved by the U. FDA to treat ALS (Riluzole, Nuedexta, Radicava, and Tiglutik).

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Comments:

18.07.2019 in 17:10 tideti:
Не знаю.

19.07.2019 in 07:07 ythelsaupo:
решил помочь и разослал пост в соц. закладки. надеюсь поднимется популярность.