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Effect of malaria in countries
Sickle Cell Anemia Research Paper
Sickle cell anemia introduction research paper
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B1.1 Where do you think you’ll find that the most villagers are dying from sickle-cell anemia? Explain.
Most villagers that are dying from sickle-cell anemia will come from the villagers at the very wet regions where there are many mosquitoes. The simulation shows that the malaria death for very wet regions rate is 0.2, that is the highest number compared to other regions. It is because there are many mosquitos in that area, so that area might be where malaria has long been endemic. Because of that, the villagers in those very wet regions have evolved dozens of chemical as defenses against malaria and the sickle cell is one of them (anti-malarial). Natural selection acts so that people with sickle cell allele are more common in those very wet regions as they survive and reproduce better in the environment where malaria is endemic, especially those people with heterozygous sickle cell allele (HbA/HbS) as it acts as ‘shield’ that protect them from dying from malarial disease and also sickle cell disease. However, those who have sickle cell allele especially the homozygous for the
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sickle cell allele have high chance to be dying with sickle cell anemia. People with homozygous HbS protected against malaria, but not sickle cell anemia, that’s why they died from sickle cell anemia but not malaria and that is why we can see lots of people dying from the sickle-cell anemia in this region. B1.2 Do you think the sickle-cell allele will disappear in any of your runs for the different regions?
Explain.
Yes, the sickle cell allele will disappear but only at the dry area where there are no mosquitoes. It is because, if we applying the natural selection theory, people with sickle cell will not have any advantage at environment that do not have or have very little cases of malaria, like the dry area that have no mosquitoes. People with sickle cell anemia at the dry area will die from the sickle cell disease, as the antimalarial properties of the sickle cell is not an advantage at the dry environment, including those that are sickle cell disease carrier. So, as the time goes by, the population with sickle cell anemia will die out and disappears, because those that did not have sickle cell allele will survive and reproduce better compared to those who have the sickle cell
allele.
This module of study has focused on many aspects of human health, anatomy, and the disease process. It has included such topics as the human organ systems, the mechanism of disease and the resulting disruption of homeostasis, the integumentary system, and the musculoskeletal system. The following case studies explore how burn classification will affect treatment, how joint injuries can disrupt mobility, and last, how a sedentary lifestyle can contribute to a decline in a person’s health status. The importance of understanding disease and knowing when to seek treatment is the first step toward enjoying a balanced and healthy life.
On Sunday, a nurse on a medical/surgical floor in a large private hospital is assigned as the primary nurse to a woman who was just admitted. The woman’s testing begins on Monday and the primary nurse does not have work for the next few days. The nurse returns on Saturday and goes over the woman’s charts. The nurse discovers that the woman has chronic lymphocytic leukemia and is being treated for the disease. After approaching the woman the nurse realizes that the woman is unaware of her diagnoses as she asks the nurse when she will be able to return to work. The nurse explains that she has not yet spoken with the physician and will get back to her once she has done so. On your way back to the nurses' station, one of the woman's two daughters approaches the nurse and urges the nurse to assure her mother that there is no reason for concern. The daughter explains that her mother has just been through a painful divorce and
Malaria survives on healthy red-blood cells and carriers do not have a lot of healthy red-blood cells. Similarly to how those with hemochromatosis starved the bubonic plague of iron, sickle cell anemia carriers starve malaria of red-blood cells. The proactive effect of malaria only works on those who have one copy of sickle cell anemia and not the actual illness. If one has sickle cell anemia, one is more likely to get malaria. Nonetheless, malaria is such a vicious disease that anything that can aid in the fight against it and towards survival and reproduction is helpful.
1. Sickle Cell Disease is life-threatening and has a risk of of causing depression. In this study I examine the experiences that Sickle Cell patients go through specifically at emergency healthcare facilities to find out if there are any negative stigmatizations surrounding this disease. There may be judgments that are made about these patients from healthcare professionals when they seek drugs for their pain relief that may cause the stigmatization to occur. I will also investigate why individuals that have Sickle Cell Disease experience longer waiting times at emergency healthcare facilities and the lack of control they may have over their care regime.
Sickle cell disease is a group of disorders that affects the blood, specifically, a molecule called hemoglobin in red blood cells (“sickle cell disease”, 2016). Hemoglobin is a molecule that facilitates the delivery of oxygen throughout the body (“sickle cell disease”, 2016). A mutant form of the hemoglobin molecule causes red blood cells to become crescent shaped or “sickled shaped” (Lonergan et. al. 2001). This distorted shape of red blood cells causes rigidity of the blood cells and vaso-occulusion (or the blood vessels to become clogged) (Rees et.al., 2010). This often leads to a low number of red blood cells (anemia), repeated infections and episodes of pain that are periodic (“Sickle cell disease”, 2016). Although sickle cell disease
In the continent Africa, about 1 in 100 individuals develops this disease. We ask ourselves why is the frequency of a potentially fatal disease so much higher in Africa? The answer is related to another deadly disease, which is called malaria. Chills, fever, vomiting, and severe headaches characterize malaria (GENETICS Sickle Cell Case Study. (n.d.). 2000, October 19). Malaria is caused by a disgusting parasite called Plasmodium that is transmitted to humans by mosquitos. When the malaria parasites invade the bloodstream, the red blood cells that contain defective hemoglobin get sickle cell out and die (Facts About Sickle Cell Disease. 2014, January 16). This helps protect the individual with Sickle Cell Anemia from an infection of malaria. As you can see, this is why a variety of areas in the world has a high rate of malaria, such as
SCD has major social and economic implications for the affected child and the families. Recurrent sickle-cell crises interfere with the patient’s life, especially with regard to education, work and psychosocial development (WHO). Sickle cell anemia, specifically, is a serious disease that can require frequent hospital stays. Repeated hospitalization for intravenous pain medication, antibiotic therapy and blood transfusions is undertaken to treat medical problems as about 1 in every 10 children with sickle cell disease. People with SCD may suffer abdominal pain, breathlessness, delayed growth and puberty, fatigue, fever, ulcers, among others. These patients often die early of overwhelming infection or as a consequence of acute or chronic damage to the body organs. Those with sickle cell disorder often suffer neglect and
Explain why the increased prevalence of sickle-cell disease among African Americans has more to do with the environmental factors than the skin color or other phenotypes used to define races.
Sickle cell anemia is a hereditary disorder that mostly affects people of African ancestry, but also occurs in other ethnic groups, including people who are of Mediterranean and Middle Eastern descent. More than 70,000 Americans have sickle cell anemia. And about 2 million Americans - and one in 12 African Americans - have sickle cell trait (this means they carry one gene for the disease, but do not have the disease itself).
The first funding for sickle cell disease began thirty years ago the federal legislation dealing with sickle cell was accepted. This legislation present notab...
Sickle cell anemia is an inherited disease of red blood cells. Normally red blood cells contain a protein called hemoglobin A, which carries oxygen to all the organs in the body. With sickle cell anemia, however, the body makes a different kind of protein, called hemoglobin S.
...creases, therefore speeding the sickling process. Sickle cells also have a shorter life span (10 - 20 days) than normal red blood cells (90 - 120 days). Every day the body produces new red blood cells to replace old ones, but sickle cells become destroyed so fast that the body cannot keep up. The red blood cell count drops, which results in anemia. This gives sickle cell disease its more common name, sickle cell anemia.
Simmon, Harvey. "Sickle Cell Disease." University of Maryland Medical Center. N.p., 14 Mar. 2013. Web. 06 Feb. 2014.
Having an inherited disease like sickle cell anemia takes a life-long of treatments and preventions of complications that comes with being diagnosed with sickle cell anemia. Many people have lived a long time while dealing with the disease because of the on-going care being provided to keep patients as healthy as possible. Knowing that both male and female have the sickle cell trait can prevent having a child with the sickle cell disease. From the help of the parents, doctors and medicine, sickle cell patients don’t have to deal with the pressure of living with a life threatening disease.
Sickle Cell Anemia seems to be one of the hardest conditions to live with due to the severity of its symptoms and it can be an encumbrance to everyday life. Although this condition is hard to live with, it is possible to live with it. Thanks to the twenty-first century advancements, there is great medical care available to patients and many other resources and support groups to help families through this harsh reality of living with sickle cell. Perhaps one day there will be a readily available cure for this horrible disease. Until then, a patient with sickle cell should have a support system and take care to live a healthy life so that they can live their life to the fullest.