Preview

Amyotrophic Lateral Sclerosis Research Paper

Good Essays
Open Document
Open Document
705 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Amyotrophic Lateral Sclerosis Research Paper
Amyotrophic Lateral Sclerosis Amyotrophic Lateral Sclerosis, also called ALS or Lou Gehrig's disease, is a genetic disease that affects the nerve cells that control muscle movement. ALS is a unique disease by the symptoms it causes when it is just beginning, the way it effects the people who have it, the people who are effected by it, and the way it is passed down from generation to generation in families. The symptoms of Amyotrophic Lateral Sclerosis are easy to overlook. The first symptoms of ALS may include twitching, cramping, stiffness, or weakness by the people who have it. Slurred speech is one of the next symptoms that will occur. Eventually, people with Amyotrophic Lateral Sclerosis will loose much of their muscle control, and they …show more content…

Ninety percent of ALS cases in people is "sporadic ALS," which means that the person did not receive the disease from anyone else in their family. The other ten percent affected have cases of "familial ALS" (FALS). FALS is passed down through families. These people may have ALS their entire life, but it will only usually show up in their lives between the ages of forty and sixty. It is rare for ALS to appear in people under the age of twenty. Unlike some other diseases, Gender does not affect the chances of receiving ALS. Males have the same chance of receiving the disease as females do. Amyotrophic Lateral Sclerosis is a unique disease because of the diverse groups of people that it can …show more content…

There are multiple ways that the ALS disease is passed down. FALS is generally autosomal dominant, which gives the affected person's children a fifty percent chance of having the disease if the parent had one normal gene and one mutated gene. ALS may also have an autosomal recessive pattern, which would require both parents to have a single mutated gene in order to pass the disease to the next generation. ALS is rarely passed down by an X-linked dominant pattern. To inherit ALS this way, the offspring ,if it is a female, needs to receive a mutated X chromosome from both parents. If the offspring is a male, only one X chromosome is needed to inherit the disease. FALS shows it's individuality by the many ways it transfers diseases from one generation in a family to the

You May Also Find These Documents Helpful

  • Good Essays

    Case Study 4

    • 1348 Words
    • 5 Pages

    Because motor neurons degenerate with ALS, they can no longer send impulses to the muscle fibers that normally result in muscle movement. Early symptoms of ALS often include increasing muscle weakness, especially involving the arms and legs, speech, swallowing or breathing. When muscles no longer receive the messages from the motor neurons that they require to function, the muscles begin to become smaller. Therefore limbs begin to look "thinner" as muscle tissue atrophies.…

    • 1348 Words
    • 5 Pages
    Good Essays
  • Good Essays

    Researchers found that ALS was commonly diagnosed in athletes. Ever since the career of Lou Gehrig a former baseball player was cut short by ALS, the disease has been forever linked to elite athletes. Lou Gehrig was a former baseball player for the NY Yankees. In 1939 Gehrig was having a hard time in his baseball career. He began to have difficulty with something as simple as tying his shoelaces. He checked himself into a Mayo Clinic, where after a series of tests, doctors informed him that he was suffering from ALS. On June 2, 1941, he passed away in his sleep at his home in New York. A team of doctors later found out that the amount to balls pitched and stuck to his head had caused head trauma to which then lead to…

    • 1273 Words
    • 6 Pages
    Good Essays
  • Better Essays

    Amyotrophic lateral sclerosis (ALS) is a deadly motor neuron disease that affects the worldwide population; it causes degeneration of the upper and lower motor neurons within the body leading to muscle atrophy of the extremities and respiratory muscles, eventually leading to respiratory failure and death. Due to…

    • 1605 Words
    • 7 Pages
    Better Essays
  • Better Essays

    ALS disease is commonly known as Lou Gehrig disease. First, Lou’s career changed rapidly when he was diagnosed with ALS. “The great New York Yankees first baseman was diagnosed with ALS in 1939 and died two years later from the progressive neuromuscular disorder” (Aebischer). This passage suggests that Lou Gehrig had a very good life playing baseball until he was diagnosed with ALS and passed away. Next, Lou Gehrig was the man who discovered ALS, he may not have been the first to have had it. “Lou Gehrig was discovered by the disease, be he made it famous” (Bumas 3). This passage implies that people may not have been too familiar with Lou before he got ALS, but he has made that disease famous. Lastly, ALS took Lou Gehrig’s life too early. "Two years after Lou was diagnosed with ALS he passed away at the age of 37" (Gehrig 4). This…

    • 1021 Words
    • 5 Pages
    Better Essays
  • Better Essays

    ALS Research Paper

    • 1608 Words
    • 7 Pages

    Amyotrophic Lateral Sclerosis (ALS), otherwise known as " Lou Gehrig's Disease ", is a devastating disease that effects the nerve cells in the brain and spinal cord. French neurologist, Jean-Martin Charcot, first discovered the disease in 1869. Attention was not brought to the disease until 1939, when New York Yankees first basemen Lou Gehrig retired because of his diagnosis (4). Specifically referred to as a "neurodegenerative disease", ALS is the lack of nourishment to muscles (5). If you break "Amyotrophic" down into its latin meanings "A" means no, "Myo" is muscle, and "Trophic" means nourishment (6). It slowly eats way at the ability to eat, speak, walk, and breath, and will eventually lead to the victims death. ALS is the most common of five motor neuron diseases: botulism, tetanus, poliomyelitis, and spinal muscular atrophy. Motor Neurons run from the brain to the brain stem, connect to the spinal cord, and from the spinal cord they reach out to the corresponding muscles (5).…

    • 1608 Words
    • 7 Pages
    Better Essays
  • Satisfactory Essays

    ALS, otherwise known as Lou Gehrig’s disease, is a disease that results in the continuous degeneration of muscle structure. Although the cause of the sickness is unknown, someone who’s parents had it are more likely to contract the disease than anyone else. About half of all ALS patients 18 months after diagnosis, while only 10 percent live longer than ten years. People can live for many years with the disease if they are placed on a ventilator. While most cases are diagnosed after the age of 50, cases have been diagnosed from ages 12 - 98 years of age. About 5,000 people are diagnosed every year in the United States. Not much is known about this ailment which makes it even more…

    • 123 Words
    • 1 Page
    Satisfactory Essays
  • Good Essays

    “Amyotrophic lateral sclerosis (ALS) is a fatal neuromuscular disease characterized by progressive degeneration of upper and lower motor neurons, which are responsible for the transmission of information form the cerebral cortex to the skeletal muscles and production of voluntary movement of the upper and lower extremities. It is associated with progressive paralysis, loss of communicative ability and functional decline”, stated (Ozanne, Graneheim, &…

    • 637 Words
    • 3 Pages
    Good Essays
  • Better Essays

    Ecstasy

    • 1456 Words
    • 6 Pages

    Duchenne muscular dystrophy is an inherited disease that is also known as muscle weakness that gets worst after a short period of time. Duchenne muscular dystrophy is caused by defected gene for dystrophy which is a protein in the muscle that is often said to be passed down from generation from family members. Duchenne muscular dystrophy is more common in people without any family history. Duchenne muscular dystrophy is known to only effect guys. Due to the way this gene in inherited, girls are not likely to inherited this disease. When women who have male kids have a fifty percent chance of inheriting Duchenne muscular dystrophy and the daughters have a fifty percent chance of inheriting this disease to their offspring when they have kids of their own. Duchenne muscular dystrophy is inherited to one out of every three thousand six hundred male infants due to this disease being inherited from family members. Duchenne muscular dystrophy is more effective to those who have a family history of this miserable disease. This condition can be very dangerous as to leaving patients to die at age twenty five due to lung disorders.…

    • 1456 Words
    • 6 Pages
    Better Essays
  • Satisfactory Essays

    Muscular Dystrophy Essay

    • 446 Words
    • 2 Pages

    Muscular dystrophy (MD) is a group of genetic diseases involving progressive weakness and degeneration of the muscles that control movement. In some forms of MD, the heart muscles and other involuntary muscles, as well as other organs, are affected. There are 9 distinct types of MD.…

    • 446 Words
    • 2 Pages
    Satisfactory Essays
  • Powerful Essays

    Als Research Paper

    • 1495 Words
    • 6 Pages

    ALS (Amyotrophic Lateral Sclerosis) or Lou Gehrig’s Disease is a classified as a degenerative neurological disorder that inhibits motor neurons in the spinal cord and brain to function properly. This disease eventually results in paralysis and imminent death over a period of time. ALS patients have anywhere from a few months, to a couple years to live after diagnosis since their nervous systems are slowly destroyed, rendering the body useless, and sustaining life impossible.…

    • 1495 Words
    • 6 Pages
    Powerful Essays
  • Good Essays

    Neurofibromatosis

    • 652 Words
    • 3 Pages

    Most commonly Neurofibromatosis is passed on by family members through genes. However, 30 to 50% of newly diagnosed people have no family history of the condition, which can be attributed to a spontaneous mutation in the gene. Once this mutation has occurred, future generation will be at risk of getting the disorder.…

    • 652 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Adrenoleukodystrophy Essay

    • 1307 Words
    • 6 Pages

    ALD affects the nervous system in the brain. The disease strips away the coating or the covering of the nerves this covering is called myelin. What causes this to happen is the accumulation of long chain fatty acids that accumulate the brain and the adrenal glands. The body normally produces these fatty acids but they are broken down by proteins in the peroxisome in cells but in people with ALD this does not happen. The most common sing that a person has ALD is personality and behavioral changes. Followed by learning disabilities, vision problems, attention deficit disorder, short and long-term memory loss, and loss of coordination or gait.…

    • 1307 Words
    • 6 Pages
    Good Essays
  • Good Essays

    Friedreich's Ataxia

    • 350 Words
    • 2 Pages

    Friedreich's ataxia is an autosomal recessive genetic disorder. This means you must get a copy of the defective gene from both your mother and father. About 1 in every 22,000-29,000 people develop this disease but family history of the condition raises your chances of getting it. On average, after 10-15 years with the disease patients are usually wheelchair bound and require assistance with all activities.…

    • 350 Words
    • 2 Pages
    Good Essays
  • Good Essays

    The Mayo clinic reports “These patients experience periods of new symptoms or relapses that develop over days or weeks and usually improve partially or completely, and then the relapses are followed by quiet periods of disease remission that can last months or even years. About 60-70 percent of people with relapsing-remitting MS eventually develop a steady progression of symptoms, with or without periods of remission, known as secondary-progressive MS (Mayo Clinic).” Patients may each experience a different set of symptoms, these symptoms depend on which portion of the brain or spinal cord is affected by the disease. According to the U.S. National Library of Medicine “Initial symptoms of MS are blurred or double vision, red-green color distortion, or even blindness in one eye (U.S. National Library of Medicine).” Additional symptoms may include numbness or weakness in one or more limbs, which typically occur on one side of the body at a given time, or in the legs and truck area, partial or complete loss of vision, usually in one eye at a time, prolonged double vision, tingling or pain in different parts of your body, lack of coordination or unsteady gait, slurred speech, fatigue, dizziness, problems with bowel and bladder function, epileptic seizures, and lastly tremors. Epileptic seizures are a rare occurrence and only occur in a minority of patients. Symptoms…

    • 994 Words
    • 4 Pages
    Good Essays
  • Good Essays

    Adrenoleukodystrophy is transmitted from parents to their children as an X-linked genetic trait. ALD is an inborn error of metabolism that causes the degeneration of the brain because of abnormally high level of fat in his blood, certain long-chain saturated fats .There is an enzyme that metabolizes these fats is defective in ALD patients. There is also liquefaction of white matter in the brain. This causes degeneration of the brain and the body loses its functions and death within two years of diagnosis.…

    • 629 Words
    • 3 Pages
    Good Essays