Top-Rated Free Essay
Preview

Evolution of Disease Sickle Cell Anemia

Better Essays
800 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Evolution of Disease Sickle Cell Anemia
Evolution of Disease

Sickle Cell Anemia
Sickle Cell Anemia is a disease that which the red blood cells form an abnormal sickle or crescents shape. Red blood cells are very important to the human body because they carry oxygen throughout the body. The main causes of Sickle cell is when the cells in the body mutate into abnormal cell called haemoglobin S. Haemoglobin S causes the red blood cells to become sickle shaped, rigid. This causes to make it more difficult for the cells to flow the vein to deliver the oxygen. Sickled cells can also stick to walls of the vein that can cause blood clotting which leads to less blood flow which can lead to organ damage, pain and infection. The disease is passed through families so people can inherit the sickle cell gene when only one parent has the sickle cell gene the child can have sickle cell trait where the child has only minor traits of the disease and like a normal life. When both parents have the sickle cell gene the child has to suffer through the symptoms of sickle cell anemia. The symptoms do not show until the person is 4 months old. Most patients that have sickle cell anemia have painful episodes called crises which can last from hours to days. The episodes are very painful especially to the bones of the back and the chest. Patents can have many crises in one year or only have one crisis per year. Some other symptoms can be fatigue, paleness, rapid heart rate, shortness of breath, jaundice (yellowing of eyes and skin), blood clotting and painful joints caused by arthritis. Sighs and tests that can diagnose sickle cell anemia are bilirubin, blood oxygen, complete blood count, serum potassium. Treatments that help manage and control the symptoms. And limit the numbers of crises. Patients with sickle cell anemia need ongoing treatment even during the time not having painful crisis. Treatments that can help are blood transfusion, pain medicines and plenty of fluids. Bone marrow or stem cell transplants can sure sickle cell anemia but are not an option for most patients because they cannot find a well-matched stem cell donor.
.Sickle Cell Trait
A person that is diagnosed with sickle cell trait is heterozygous meaning that they may maybe minor symptoms but usually do not because they have enough normal cells to live a normal life without being worried have having attacks or complication. However it has been found that people who have sickle cell trait have asthma. When people are in an environment that has Malaria they get infected but people who have sickle cell do not the same goes for people that have sickle cell trait. The reason why Malaria infectious disease is attacks the red blood cells in order to breed and survive within the body. People who have sickle cell trait have both normal and abnormal cell therefore, Malaria does not affect their body due to limited sources.
Evolution of Sickle Cell Anemia
In 1904, a man traveled from Grenade to the United States to study in Dental Sugary. A couple months later the man was admitted into a hospital in Chicago where he developed severs respiratory distress and led ulcer both are symptoms of sickle cell. Dr. Earnest E. Irons performed a routine blood test and urine test and found “pear shaped, elongated” sickled blood cells in the man bloods. Not until 1910 Dr. James Herrick the supervisor of Dr. Irons published an article describing the blood cells of this patient. This was the first documented and recorded case of sickle cell in western medicine. In 1915 the third case of sickle cell was described during this time Dr. V Emmel suggested that the diseases had a genetic basis.

CITATION

Sickle Cell Trait: Disease or Evolutionary Advantage." Sickle Cell Trait: Disease or Evolutionary Advantage. N.p., n.d. Web. 08 Oct. 2012. <http://students.cis.uab.edu/slawrenc/SickleCell.html>.
Board, A.D.A.M. Editorial. Sickle Cell Anemia. U.S. National Library of Medicine, 18 Nov. 0000. Web. 08 Oct. 2012. <http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001554/>.
"Sickle-Cell Disease History." Sickle-Cell Disease History. N.p., n.d. Web. 08 Oct. 2012. <http://www.news-medical.net/health/Sickle-Cell-Disease-History.aspx>.
"A History of Sickle Cell Disease - The Sickle Cell Association of Ontario." A History of Sickle Cell Disease - The Sickle Cell Association of Ontario. N.p., n.d. Web. 08 Oct. 2012. <http://www.sicklecellontario.org/sickle-cell-101/a-history-of-sickle-cell-disease>.
"What Causes Sickle Cell Anemia?" - NHLBI, NIH. N.p., n.d. Web. 08 Oct. 2012. <http://www.nhlbi.nih.gov/health/health-topics/topics/sca/causes.html>.

You May Also Find These Documents Helpful

  • Good Essays

    1. Sickle cell disease is a group of disorders that affects hemoglobin, the molecule in red blood cells that delivers oxygen to cells throughout the body. People with this disorder have atypical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape.…

    • 819 Words
    • 4 Pages
    Good Essays
  • Powerful Essays

    | |Risk Assessment: Risk for infection r/t Sickle Cell Disease; Risk for fluid and electrolyte imbalance; Fall risk; Braden Score: 22 |…

    • 1076 Words
    • 5 Pages
    Powerful 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
  • 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
  • Powerful Essays

    Sickle cell disease is an inherited disorder in which red blood cells are abnormally shaped. This abnormality can result in painful episodes, serious infections, chronic anaemia, and damage to body organs.…

    • 1612 Words
    • 7 Pages
    Powerful Essays
  • Good Essays

    The core reading for this week included an excerpt that read “…the first cases of sickle cell disease were mostly amongst Africans and African Caribbeans. Racial thinking led to the assumption that sickle cell disease was a ‘Black disease’, even though many African people are not at risk for these disease and many carriers are not African” (Russell, 2014, p. 69). This, for me, was very insightful and enlightening, as it presents a way of thinking that is not common or taught in our society. It brought me to the realisation that our society has conditioned us to believe that ‘racial diseases’ could be a real thing, when in actuality, ‘racial diseases’ is simply a notion derived from migration. There have been so many instances wherein certain…

    • 574 Words
    • 3 Pages
    Good Essays
  • Powerful Essays

    Sickle Cell Anemia

    • 1567 Words
    • 5 Pages

    Sickle cell anemia or also known as sickle cell disease is a hereditary genetic disease defined by the presence of odd shaped crescent-shaped red blood cells instead of the regular round disc like shape cells. Red blood cells transport oxygen from the lungs to various other organs and tissues with the help of a protein called hemoglobin. The main cause of sickle cell disease is when hemoglobin mutates into an abnormal type called hemoglobin S. The presence of Hemoglobin S causes red blood cells to be sickle-shaped and rigid, making it more difficult for them to flow through blood vessels in the body to deliver oxygen. Therefore, the sickled cells latch onto the walls of various blood vessels throughout the body, resulting in blocked blood flow that can lead to organ damage, pain and infections…

    • 1567 Words
    • 5 Pages
    Powerful Essays
  • Good Essays

    Sickle cells anemia is a form of condition which the blood has lower number of red cells. Sickle cell anemia does not affect many infants until after four months of age. Some individuals have mild symptoms such as shortness of breath, dizziness, headaches and coldness in…

    • 490 Words
    • 2 Pages
    Good Essays
  • Good Essays

    Sickle Cell Anemia

    • 568 Words
    • 4 Pages

    the supply of oxygen gets cut off. A normal blood cell lives up to 120…

    • 568 Words
    • 4 Pages
    Good Essays
  • Good Essays

    Sickle Cell Anemia

    • 1657 Words
    • 7 Pages

    Sickle Cell Anemia, also known as Sickle Cell Disease, is a disease that causes the production of abnormal hemoglobin. The red blood cells (RBCs) carry oxygen to organs and tissues. Hemoglobin, a molecule in the RBCs, is a protein that attaches to the oxygen in the lungs and carries it to all parts of the body. Hemoglobin takes on the oxygen, and releases carbon dioxide, a process known as oxygenation. In the tissues, deoxygenation occurs where the processes is reversed, when hemoglobin releases oxygen and takes on carbon dioxide. When the RBCs are healthy, they can easily move through the tiniest blood vessels throughout the body because of their flexibility. The hemoglobin S is fragile and abnormal in Sickle Cell Anemia, and the RBCs are pointy with a shape like the alphabet letter "C" or the crescent moon. This makes the RBCs difficult to move pass through the blood vessels. The RBCs become hard, and can get stuck in blood vessels, and often clog the spleen. This causes pain, infection, and poor blood flow in patients that have Sickle Cell Anemia. The RBCs also block blood flow to organs, such as the heart, lungs, brain, etc., which can lead to stroke, damage to organs, especially the spleen, acute chest syndrome, disability, and sometimes, even death.…

    • 1657 Words
    • 7 Pages
    Good 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
  • Powerful Essays

    "An ISU student died March 12 from complications of Sickle Cell Anemia…there is no cure for Sickle Cell Anemia" (Indiana Statesman, 2004). What is Sickle Cell Anemia? According to National Institute of Health, Sickle Cell Anemia is a lifelong, inherited blood disorder or disease, characterized primarily by chronic anemia and periodic episodes of pain. It is one form of sickle cell disease, a category of blood disorders caused by defective hemoglobin. Hemoglobin is a substance in all red blood cells that enables them to carry oxygen from the lungs, through the bloodstream, to all parts of the body (systemic circulation). With Sickle Cell Anemia, the hemoglobin in the red blood cells is defective, instead of being smooth and donut or disc-shaped, the red blood cells become stiff and sickle-shaped. Therefore, organs and tissues are deprived of oxygen-rich blood, which produces periodic extreme episodes of pain and permanent damage to vital organs (NIH, 1987). The shape of the cell resembles that of a narrow curved blade or "sickle" that is used in cutting grasses -that is how the condition got its name (USDHEW, 1989).…

    • 3212 Words
    • 13 Pages
    Powerful Essays
  • Satisfactory Essays

    Causes Of Sickling

    • 93 Words
    • 1 Page

    Sickling of the cells can lead to other symptoms such as fatigue and anaemia, dactylitis (swelling and inflammation of the hands/feet) and arthritis, bacterial infections, splenic sequestrations (sudden pooling of the blood in the spleen) and liver congestion, lung and heart injury and aseptic necrosis. Normal haemoglobin cells are smooth and round in shape like the letter "O." These cells flow freely within the blood vessel. Abnormal haemoglobin cells deform like the letter "C," losing oxygen and clot together blocking the blood flow and stopping the movement of a healthy, normal, oxygen-carrying blood.…

    • 93 Words
    • 1 Page
    Satisfactory Essays
  • Good Essays

    Sickle Cell Disease

    • 1110 Words
    • 5 Pages

    Sickle cell anemia is caused by an abnormal type of hemoglobin called hemoglobin S due to the replacement of a non-polar valine amino acid for a polar glutamic acid at the seventh position of beta chain. This substitution produces a net of decrease in negative charge; thus, it changes the molecule’s electrophoretic mobility. Hemoglobin S distorts the shape of red blood cells, especially when exposed to low oxygen levels. The distorted red blood cells are shaped like…

    • 1110 Words
    • 5 Pages
    Good Essays
  • Better Essays

    biology project

    • 1564 Words
    • 6 Pages

    Episodes of pain. Periodic episodes of pain, called crises, are a major symptom of sickle cell anemia. Pain develops when sickle-shaped red blood cells block blood flow through tiny blood vessels to your chest, abdomen and joints. Pain can also occur in your bones. The pain may vary in intensity and can last for a few hours to a few weeks. Some people experience only a few episodes of pain. Others experience…

    • 1564 Words
    • 6 Pages
    Better Essays

Related Topics