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

  • 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
  • Satisfactory Essays

    Charles Darwin’s theory states that the change in evolution is the variation in each generation and different individual surviving features with different combinations of the variable. The Individuals with characteristics that increase their probability of survival will be able to reproduce more often and their offspring will also benefit as there would be an advantage because it would be passed on to the offspring. Over time these variation of characteristics will spread through the population. (College, 2009)…

    • 594 Words
    • 2 Pages
    Satisfactory 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

    Consider the pedigree analysis of sickle-cell disorder. Could two normal parents have a child with sickle-cell anemia?…

    • 435 Words
    • 5 Pages
    Satisfactory 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
  • Good Essays

    Sickle Cell Lab

    • 1314 Words
    • 6 Pages

    When Malaria is present and infects red blood cells, parasites can infect cells carrying defective hemoglobin which may result in death. Allele frequency changes over time depending on the pressures or circumstances facing a particular population. African populations are especially impacted by both malaria and sickle cell anemia. Depending on the impacted population, allele frequency often shifts and well suited organisms are likely to survive and allele frequencies can increase. When a population is effected by disease or other circumstances, allele frequency may decrease or change. HbA (normal hemoglobin) and HbS (defective hemoglobin) have varying frequencies and while the HbS gene is present in populations it is important to understand how Malaria in particular can affect the sickle cell frequency. The way that diseases such as malaria impact the HbS gene may be different than how populations unaffected by malaria are impacted by HbS. What will happen to the sickle cell frequency in the presence of Malaria?…

    • 1314 Words
    • 6 Pages
    Good Essays
  • Good Essays

    Sickle cell disease is much more common in people of African and Mediterranean descent. It is also seen in people from South and Central America, the Caribbean, and the Middle East. Sickle cell anemia is caused by an abnormal type of hemoglobin[->0] called hemoglobin S. A single cell causes this disease. Hemoglobin is a protein inside red blood cells that carries oxygen. The fragile, sickle-shaped cells deliver less oxygen to the body’s tissues, and also get stuck more easily in small blood vessels, as well as break into pieces that can interrupt healthy blood flow. These problems decrease the amount of oxygen flowing to body tissues even more, sometimes causing a crisis.…

    • 789 Words
    • 4 Pages
    Good 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
  • Good Essays

    Survival of the Sickest

    • 850 Words
    • 4 Pages

    Survival of the Sickest, written by author Dr. Sharon Moalem, is a book discussing why evolution has not allowed for the destruction of certain diseases. He states that these deadly diseases, such as Anemia, Hemochromatosis, and High Cholesterol, are in fact tools that evolution used to help the human race survive. He explains how these diseases helped fight against more dangerous and life threatening sicknesses such as, Malaria, the Bubonic Plague, and Vitamin D deficiency related illnesses. The main idea of this book is a simple one. Evolution did not necessarily favor adaptations that made us better. Instead, it favored adaptations that helped us survive. Even if these adaptations would end up killing us in the long run.…

    • 850 Words
    • 4 Pages
    Good Essays
  • Better Essays

    cell Disease and Sickle-cell Trait, Revised Third Edition. Hilton, 2011. Print. www.medterms.com/script/main/art.asp?article key=9368, n.d. Web. 20 Apr. 2013.…

    • 1165 Words
    • 5 Pages
    Better Essays
  • Satisfactory Essays

    inheritance problems

    • 934 Words
    • 4 Pages

    Figure 1 A pedigree diagram showing the occurrence of sickle cell anaemia within one family.…

    • 934 Words
    • 4 Pages
    Satisfactory Essays
  • Good Essays

    Sickle Cell Anemia

    • 621 Words
    • 3 Pages

    Sickle cell anemia is an inherited blood disorder, identified by the sickle shape of red blood cells which carry less oxygen and break easily, causing anemia. The sickling trait, the less serious form, occurs from the inheritance of only one parent; however, both parents must exhibit the disease in order for full symptoms to take place. It is caused by an error in the gene that tells the…

    • 621 Words
    • 3 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
  • Good Essays

    Natural selection favored brown bunny alleles due to its ability to survive and reproduce. The four forces of evolution also impact human evolution. An example is a natural selection affecting Malaria. People with the Malaria gene tend to have one sickle cell allele and a normal cell allele. Since they have two different alleles they better adapt to live in Malaria zones than people with normal blood or sickle cell genes. Therefore, people who carry the Malaria allele are favored by natural selection in Malaria zones, will survive and…

    • 301 Words
    • 2 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