Preview

sickle cell disease

Satisfactory Essays
Open Document
Open Document
507 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
sickle cell disease
‘How could natural selection increase the number of children born with sickle-cell disease in certain regions when these individuals are unlikely to survive and produce offspring?’

Darwin’s theory proposes that 3 conditions are a requisite for natural selection to occur. They are a struggle for existence of the offspring as they are competing for limited resources, variation within species which gives some individuals advantage over others hence better chance of survival and lastly inheritance of advantageous characters to offspring which over successive generations will be common in the population helping survival of fittest over those without. This could in effect lead to change in character from one generation to the next.
In the case study the sickle cell carriers have an advantage over non carriers as in those regions a great cause of death is malaria. The sickle cell carriers seem to have some resistance to malaria and therefore survive to produce offspring, those advantageous characteristics pass on to the descendants in this case the heterozygous gene for sickle cell, the descendants will in turn be resistant to malaria and therefore have a greater probability of surviving to produce offspring as well with the advantageous sickle cell gene. The successive generations will carry on in this manner and be prevalent as the fittest depending on a higher number of successful individuals in relative to number of survivors of other individuals, the relative number of individuals that have higher fitness than others and the fact that they must reproduce.
Some regions in Africa have higher malaria risks in which selection pressure mean that number of individuals with the mutant gene for sickle cell will be higher as they will be resistant to the malaria and survive to adulthood and reproduce in comparison to the number of those individuals who although not carriers of sickle cell disease managed to survive and reproduce. Most of the non-sickle cell carriers

You May Also Find These Documents Helpful

  • Satisfactory Essays

    Sickle cell is the absolute disease, and sickle trait is someone who may carry the trait for the disease which may mean, if they were to have a children they could perhaps get the disease.…

    • 767 Words
    • 4 Pages
    Satisfactory Essays
  • Satisfactory Essays

    In looking at sickle-cell anemia, we are interested in studying the gene that codes for…

    • 435 Words
    • 5 Pages
    Satisfactory Essays
  • Good Essays

    Bilogy 3 Research Paper

    • 921 Words
    • 4 Pages

    Sickle cell anemia affects people with African, Mediterranean, Middle Eastern, and Indian ancestry (Scientific American). Sickle cell anemia occurs when a person inherits two sickle cell gene, one from each parent, that cause the red blood cells to change and become crescent shaped. The underlying problem involves hemoglobin, a component of the red blood cells. Hemoglobin is a protein molecule in red blood cells that carries oxygen from the lungs to the body’s tissues and returns carbon dioxide from the tissues to the lung. In sickle cell anemia, the hemoglobin is flawed (The New York Times). As a result, the cells become sickle shaped and can’t travel as easily through blood vessels. Sickle cell anemia is an illness, which has one primary cause, but a variety of symptoms and treatments (Scientific American.) Like some illnesses, sickle cell anemia has one primary cause. In order for sickle cell anemia to occur is when a sickle cell gene have, been inherited from both the mother and the father, so that the child has two sickle cell gene. The sickle cell gene causes the body to make abnormal hemoglobin. As mentioned above, hemoglobin is a protein molecule in red blood cells that carries oxygen from the lungs to the body’s tissues and returns carbon dioxide from the tissues to the lungs. A person with normal red blood cell will have hemoglobin A; however, a person with sickle cell disease will have hemoglobin S…

    • 921 Words
    • 4 Pages
    Good Essays
  • Good Essays

    Cultural and biological anthropologists have observed that people from India, Asia, and the Mediterranean have a higher percentage of people with one abnormal hemoglobin allele, compared to in other parts of the world where most people have two normal hemoglobin alleles. It's been found that people with two abnormal hemoglobin alleles carry a disease called sickle cell anemia; this disease is known to be circumstantially fatal. In addition to this finding, there's a direct correlation between the number of people in an area where the sickle cell trait is common and the amount of people with the one abnormal allele that proves to shield the infection of malaria. This single abnormal hemoglobin allele is known as hemoglobin S, Allison (1990) was first to examine that when hemoglobin S is present, people seem to be less resistant and protected against malaria. Her research in The Anthropology of Infectious Disease helps in further understanding the connection between a cultural environment where a certain disease (malaria) is most present, and how biologically people of the surrounding community anatomically adapt to fight off the condition. Natural Selection (Peters-Golden,H. 2010), the idea of how anatomical changes are largely due to favored adaptations for proficiency of survival in a given environment, can further prove why people in areas more prone to sickle cell anemia…

    • 838 Words
    • 4 Pages
    Good Essays
  • Good Essays

    Into the Jungle Ch.8

    • 522 Words
    • 3 Pages

    1) How did Tony Allison’s early life experiences in Kenya prepare him to make the discovery of the sickle cell-malaria link?…

    • 522 Words
    • 3 Pages
    Good Essays
  • Satisfactory Essays

    Sickle Cell Plan of Care

    • 610 Words
    • 2 Pages

    Sickle cell anemia is the most common form of sickle cell disease which is an inherited, autosomal recessive disorder that causes an abnormal hemoglobin cell. The person with this specific disorder inherited hemoglobin S from both parents, also known as homozygous (Lewis, Dirksen, Heitkemper, & Bucher, 2014, pp. 644-647). This hemoglobin S results from the substitution of valine for glutamic acid on the B-globin chain of hemoglobin, and this ultimately causes the erythrocyte to stiffen and elongate taking a sickle shape in response to low oxygen levels (Lewis et al., 2014, pp. 644-647). Due to the sickle cells elongated shape, and its stiff and sticky consistency it tends to get stuck in capillaries and vessels, and blocks blood flow to limbs and organs (Lewis et al., 2014, pp. 644-647). The major problems with sickle cell anemia is due to their sickled shape, reduced life expectancy and their ability to carry enough hemoglobin or transport it properly to…

    • 610 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    What happened to the frequency of the HbA allele & the HbS allele over the course of this experiment?…

    • 774 Words
    • 4 Pages
    Good Essays
  • Satisfactory Essays

    Maple Syrup Urine Disease

    • 432 Words
    • 2 Pages

    - MSUD is related to natural selection because the Infants that have homozygous dominant are selected against and they will die at a young…

    • 432 Words
    • 2 Pages
    Satisfactory Essays
  • Powerful Essays

    changes over time

    • 953 Words
    • 4 Pages

    A genetic human disease for example Huntingdon’s Chorea or Sickle Cell Anemia that illustrates higher prevalence in particular regions of the world…

    • 953 Words
    • 4 Pages
    Powerful Essays
  • Good Essays

    Sickle Cell Anemia

    • 1001 Words
    • 5 Pages

    Sickle cell disease is an autosomal recessive genetic disorder most common in African Americans, which results from a mutation affecting the amino acid sequence of the beta chains of hemoglobin molecules in red blood cells. The abnormal hemoglobin which causes the red blood cells to sickle is called hemoglobin S. Sickling occurs when the red blood cells are deoxygenated causing the cell to have a hard curved crescent shape. Due to their shape the sickle cells can become trapped in blood vessel walls causing a circulatory blockage and could cause tissues to become oxygen deprived, pain, infection, and organ damage. Red blood cells in sickle cell disease also have a life span of 10 to 20 days compared to normal red blood cells of 120 days; because of this shortened life span chronic hemolytic anemia occurs (Thompson, 2012). All together sickle cells disease causes a dramatic decrease in the quality of life that can lead to early death, the absolute need for medical intervention, and transplantations.…

    • 1001 Words
    • 5 Pages
    Good Essays
  • Good Essays

    Blood Disorders

    • 466 Words
    • 2 Pages

    * Lily, a 4-year-old Caucasian female, has she been complaining of being tired all the time. She is pale and is a picky eater. Her mother is a single mom with a small budget to feed a large family. Lily eats only pasta, breads, and hot dogs, and she drinks only artificial fruit punch. Lily has iron deficiency anemia. Infants can be infected from the time of birth from certain forms of anemia. Certain forms of anemia are hereditary. When girls are not getting the proper amount of iron in their diet then they may become iron deficiency. There are many different symptoms of iron deficiency anemia but the most common are swelling of the tongue, drying of the lips, and eating and craving ice. Lily’s mother cannot afford the proper food filled with iron so the best thing that she can buy for Lily is foods and drinks that have vitamin C in it, such as orange juice.…

    • 466 Words
    • 2 Pages
    Good Essays
  • Better Essays

    Blood Disorders

    • 724 Words
    • 3 Pages

    Sickle cell is inherited and is normally only found in Black Americans. The blood cells are shaped differently and it due to a genetic defect. (WebMD, 2014) This causes the blood cells to eliminate themselves rather quickly causing lack of oxygen to the organs in the body. The reason this disease is so painful is because the blood cells become trapped in the blood vessels. (WebMD, 2014)…

    • 724 Words
    • 3 Pages
    Better Essays
  • Good Essays

    Sickle Cell Anemia

    • 2034 Words
    • 6 Pages

    There have been many researches and tests done on the genetic causes of Sickle Cell Anemia and how it developes, as well as it's effects on the circulatory, muscular, and respiratory systems, as well as it's effects on the joints and other systems of the body, and the complications associated with them. Most of the research has been done to explore on the reasons why it mostly effects the African-American community and people who are from the West Coast of Africa. It has also been known that Sickle Cell Anemia also effects people from the Mediterranean countries (Wethers, 2000)…

    • 2034 Words
    • 6 Pages
    Good Essays
  • Good Essays

    The Sickle Cell Crisis

    • 547 Words
    • 3 Pages

    There are ways to prevent episodic sickle cell crisis such as staying adequately hydrated, limiting physical activities, blood transfusions and taking medication such as hydroxyurea. In Addition, one of the biggest issue with Sickle cell anemia is lack of funding which is due to the fact that it is not officially recognized as a health disparity topic by CDC. Another disparity is the fact that in terms of funding and treatment; SCD pales in comparison to other diseases. the funding disparities for research on sickle cell drugs and cures compared to other pediatric diseases such as Cystic fibrosis. “Cystic fibrosis a disease that affects primarily Caucasians and affects only a third of the numbers of people compared to Sickle cell but still…

    • 547 Words
    • 3 Pages
    Good Essays
  • Good Essays

    More recently, researchers have begun to make progress on understanding the mechanisms that create resistance to the lethal infection. About one out of ten African-Americans has the sickle cell mutation; are known not to develop sickle cell anaemia, leading rather normal lives. However, researchers found that these individuals, who are said to carry the sickle cell trait have an advantage (heterozygous advantage) over people who carry no copies of the sickle cell allele. A single copy of the sickle cell allele increase resistance to malaria…

    • 85 Words
    • 1 Page
    Good Essays