What is amyotrophic lateral sclerosis essay

When muscles in the torso wall and diaphragm fail, people cannot breathe without ventilator support.

Amyotrophic Lateral Sclerosis

Other causes are hypothesized to be from neurotoxicity of various metals, foods, or chemicals. Our writers can write any custom essay for you! Lou Gehrig is one of the most famous men to experienced the disease.

It targets the motor neurons that allow you to make voluntary movements and it effects your muscle strength. The thing that makes us different is the genetic sequence.

Amyotrophic Lateral Sclerosis Lou Gehrig's Disease

ALS is a fatal disease which may run its course in a period of months or over a number of years. To do that, we've trained a super-helpful Customer Support Team, ready to resolve any problems that could possibly occur during our work with your order.

Amyotrophic Lateral Sclerosis

According to Reichenberg, "the EMG will demonstrate damage due to LMN loss in the weakened muscles and may also show changes in muscles that are still strong.

Engine neurons go from the mind to the spinal cord and the muscles dispersed throughout the body.

Causes of Amyotrophic Lateral Sclerosis (ALS)

Research at this time is in the earliest of stages and is not considered a replacement for human embryonic stem cell research, but I think it holds great promises because they can differentiate and not produce cancer.

Researchers have been studying whether a defective metabolism of glutamate, an amino acid, is detrimental to the nerve cells in the muscles of ALS patients. This is demonstrative of the life-cycle for a disease that works its way through the body, eventually resulting in the failure to control basic life functions.

The other aspect of the treatment process with stem cells for amyotrophic lateral sclerosis is the transplantation. Particularly, Waller indicates that "atrophy of the anterior horn cells and replacement of the large motor neurons by fibrous astrocytes gliosis causes the affected anterior and lateral columns of the spinal cord to become hard, hence the term 'lateral sclerosis.

The BBB protects the brain from invasion and delivering cells to the brain is a challenge, but research with a mouse model for ALS done by Zhang demonstrated how this obstacle can be bypassed. Yet he is still living and doing the most he can with his life. Englanders and Australians call it Engine Neurone Disease.

These are painful and dangerous surgical procedures that require careful scrutiny because of the fragility of ALS patients.

ALS more than often strikes people between forty and sixty years, but sometimes young and old people can also develop the disease. Hum-molgen, The motor neurons affected by ALS are also known as anterior horn cells since they are located in the anterior, or front, of the spinal cord.

Pathophysiology The pathogenesis is unclear, but there are three general types of ALS: Victims can also receive a spinal tap, a MRI, or even a family background check to see if there is any history of ALS in the family. Tetanus - words Tetanus is a potentially life-threatening disease, usually associated with infected puncture wounds.

The average life span after diagnosis are three to 10 years, although 20 percent of those affected will outlive their prognosis by a number of years.

Retrieved January 24,from http: Therefore, the heart and digestive system are not involved with ALS. Cheng Zhang and colleges successfully made multiple transplantations of human marrow stem cells through the central nervous system improving motor performance and prolonging the life of superoxide dismutase SOD1 transgenic mice.

Your motor neurons slowly deteriorate, causing your muscles to not receive information from your brain. All the reference material will be cited and appropriately formatted.

SOD1 dysfunction in Amyotrophic Lateral Sclerosis Essay

However, only a small percent of these with ALS will live for ten or more years. Amitriptyline Elavildoxepin Sinequanand imipramine Tofranil have similar effects in providing antidepressant and antisialorrheic actions and provide nocturnal sedation, help potentiate analgesia and possible weight gain.Advancing ALS Research The world is our lab.

With your support, The ALS Association’s TREAT ALS™ research program fuels global collaboration to expedite the discovery of treatments and a cure for amyotrophic lateral sclerosis (ALS).

Abstract We discuss physician aid in dying, euthanasia, and other dimensions of palliative care decision making and define relevant terms raised by this case of a dying patient with amyotrophic lateral sclerosis in Washington State who is unable to self-administer a lethal prescription.

We guarantee you plagiarism-free paper. All our writers are conversant with all styles of writing. Additionally, we use academic sources and real references without cooking around figures, which is a common problem with other writing services. Als Research Paper.

als research paper - Amyotrophic lateral sclerosis (ALS), commonly known as Lou Gehrig’s disease, affects approximately 20, - 30, U.S. citizens, with an estimated 5, new diagnoses made each year. Amyotrophic Lateral Sclerosis (ALS) is a disease that causes muscles to stop working.

ALS is a rare disease found mostly in very active people. Multiple sclerosis (MS) and amyotrophic lateral sclerosis (ALS) are different diseases with some similar features and symptoms.

They both: Affect your muscles and your ability to move your body.

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What is amyotrophic lateral sclerosis essay
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