Sickle Cell Anemia Effect

Superior Essays
Sickle Cell Anemia is an inherited blood disorder that mostly affects people of African ancestry, but it can also occur in other ethnic groups such as Middle East and Mediterranean descent (National Institute of Health). The disease affects the hemoglobin molecule in the red blood cells. Hemoglobin helps with carrying oxygen from the lungs and delivering it to different parts of the body. The mutation of this disease makes the cells become abnormal and irregular shaped. As a result, the abnormal crescent shape can block the blood flow in parts of the body which causes pain and organ damage (National Institute of Health). According to the Center for Disease Control and Prevention, it is estimated that Sickle Cell Anemia affects 90,000 to 100,000 …show more content…
The most common symptom related to anemia is feeling very tired and weak. Other signs and symptoms of anemia include jaundice, shortness of breath, leg ulcers, coldness in the hands and feet, and headaches (Makani, Ofori-Acquah, Nnodu, Wonkam, Ohene, 2013). Another common side effect to having this disease is having sudden bursts of pain throughout the body. This pain is known as sickle cell crisis, and the crisis affects the body’s joints, lungs, abdomen, and bones. Sickle cell crisis can be categorized into acute and chronic crisis. Acute Sickle Cell crisis is when the pain is short and can last for hours or a week. Chronic Sickle Cell Anemia is when a patient can have pain for months and the chronic pain usually it felt from their bones. Acute and Chronic crisis occur in patients with this disease because the red blood cells that are irregular shaped, “sickled” and crescent shape block the blood flow to the limbs and the organs (National Institute of Health). This is why people experience pain with this …show more content…
The Mediterranean Journal of Hematology and Infectious Disease states “heterozygotes for the sickle gene are relatively protected against the danger of dying of malaria, as now firmly established through a number of clinical field studies from different parts of Africa” (Luzzatto, 2012). This means that patients with the defective hemoglobin that causes Sickle Cell Anemia are protected from Malaria. There are two reasons why the sickle cells help protect against the malaria disease. One reason is since the sickle cells have a short life span, the parasites are unable to survive. The second reason is that the sickled red blood cells do not contain enough nutrients for the parasite to survive the parasite usually

Related Documents

  • Improved Essays

    The body is continuously making red blood cells to replace the old ones. When a person has sickle cell disease, the body may have difficulty creating new red blood cells at the rate with which they are being destroyed. “Because of this, the number of red blood cells is usually lower than normal,” which is a condition called anemia (U.S. Department of Health…,…

    • 603 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    Chi Square Test Lab Report

    • 2147 Words
    • 9 Pages

    Sickle cell disease is an inherited disorder that is caused by a mutation in the DNA sequences that codes for the beta chain of the hemoglobin protein. Red blood cells are, normally, flexible and round, but with the sickle cell anemia the red blood cells become sticky, rigid, and crescent shaped. The Hemoglobin protein carries oxygen in the red blood cells throughout the body. With the disease, the blood cell’s shape can cause them to get lodged in the blood vessels resulting in the obstruction of blood flow, especially in the smaller arterial vessels in the body This occurrence not only reduces oxygen content to the area of concern, but can be a very painful experience for the victim. People who inherit this disease have two abnormal hemoglobin…

    • 2147 Words
    • 9 Pages
    Improved Essays
  • Improved Essays

    I am in support of the “Sickle Cell Disease Research, Surveillance, Prevention, and Treatment Act of 2015.” Sickle Cell is a serious blood disorder that causes red blood cells to become misshaped. These abnormally shaped red blood cells can get clustered into blood vessels and block blood flow to areas of the body. According to the center of disease and control the number of people with sickle cell in the united states is unknown, but it is prevalent amongst African-Americans occurring in 1 out of 365 births.…

    • 800 Words
    • 4 Pages
    Improved Essays
  • Decent Essays

    11% of patients with sickle-cell disease have had a stroke by the age of 20 years. Once a stroke has occurred, the risk of recurrence is more than 60%. - In studies in which MRI is used, up to 20% of children with sickle-cell disease have silent brain infarcts. Silent infarcts are linked to neurocognitive problems, fits, and risk of further brain infarction. -Intracranial bleeds occur in patients of all ages, but are most common between the ages of 20 years and 30 years; cerebral aneurysms.…

    • 317 Words
    • 2 Pages
    Decent Essays
  • Improved Essays

    Cells with sickle cell disease are hard and easily stick to each other. When the cells lose their oxygen, they take on the shape of a sickle or crescent. The cells stickiness can block small blood vessels and the flow of normal oxygen-carrying blood. This can cause varying levels of pain. According to sicklecelldisease.org, normal red blood cells can live up to 120 days.…

    • 656 Words
    • 3 Pages
    Improved Essays
  • Superior Essays

    The Gale Encyclopedia of Alternative Medicine stated that the genetic mutation associated with sickle-cell anemia occurred thousands of years ago and continued to pass down through generations. The mutation holders were less likely to be affected by malaria (Kapes, 2009). More research on the effects of sickle-cell anemia and malaria was conducted by Dr. Allison of the British Medical Journal. He found studies in Northern Rhodesia, an area greatly affected by malaria, that indicated a positive connection between sickle-cell anemia and malaria. 9.8 percent of sicklers had…

    • 1478 Words
    • 6 Pages
    Superior Essays
  • Improved Essays

    The Crescent Moon Disease: Sickle Cell Sickle cell anemia is a disease that is passed throughout families. Sickle cell affects the red blood cells, which cause the blood cells to look like a crescent moon instead of looking like a disc, like the photo included above. There are two types of Sickle cell: Sickle Cell Anemia and Sickle Cell- Hemoglobin C. Sickle Cell Anemia is the less severe one out of the two. Sickle Cell Anemia affects many racial and ethnic groups. One in four hundred African-American newborns have this disease in the United States.…

    • 788 Words
    • 4 Pages
    Improved Essays
  • Improved Essays

    Pain crisis is the primary symptom of SCD; it is caused by sticky, sickle cells forming blood clots resulting in ischemia. Acute chest syndrome is a potentially life-threatening complication that occurs when blood clots collect in the small blood vessels that supply the lungs. Symptoms include fever, chest pain, dyspnea, chills, and hemoptysis. Pulmonary infiltrates are common as well as pulmonary hypertension, and the majority of patients are hypoxemic (Paul, Castro, Aggarwal, & Oneal, 2011). Splenic sequestration is another common complication; rising when the sickle cells become clogged and are trapped in the spleen causing rapid splenomegaly and pain (National Heart, Lung and Blood Institute, 2015).…

    • 1703 Words
    • 7 Pages
    Improved Essays
  • Improved Essays

    Sickle Cell Research Paper

    • 1293 Words
    • 6 Pages

    The most common problem is the sickle cell shaped red blood cells that get stuck to the blood vessels, blocking blood flow, in results causing certain conditions. One condition is Hand-Foot syndrome, which is, when the foot and hand have pain, swelling and fever. Another condition is “sickle cell crisis”, this is a painful symptom that a person experience sudden body, organ and joint pain. This is due to when the sickle blood cells block oxygen flow to the tissues. This crisis can last a few minutes to weeks causing the patient to be hospitalized.…

    • 1293 Words
    • 6 Pages
    Improved Essays
  • Improved Essays

    This is a disease that gets worse with time, treatments only help lessen complications or prevent them. Treatment options for people vary depending on how bad their condition is. A stem cell transplant would essentially cure a person with the disease, most people do not meet the qualifications for a transplant and even at that, the procedure is still very risky. Usually the first symptom people with Sickle Cell experience, one of the least severe, is swelling in their feet and hands, caused by blockage in the blood vessels. To treat the swelling, pain medicine is usually prescribed and a doctor will recommend an increase in fluids, drink more water.…

    • 903 Words
    • 4 Pages
    Improved Essays
  • Superior Essays

    Sickle Cell Anemia is an inherited blood disorder of the red blood cells, which is passed down through families. Sickle cell anemia primarily affects people with African, Mediterranean, Middle Eastern, and Indian ancestry. About 70,000 children are affected with sickle cell anemia because it directly attacks their gene, it is prevalent in African-American and millions of people carry the gene. There are different types of sickle cell disease, People who inherit two sickle cell genes, one from each parent have a type of sickle cell disease called SS, it’s commonly called sickle cell anemia and is usually the most severe form of the disease. People who inherit a sickle cell gene from one parent and a gene for another type of abnormal hemoglobin, from the other parent have a different type of sickle cell disease and some types of sickle cell disease are very severe and the disease affects each person differently.…

    • 1173 Words
    • 5 Pages
    Superior Essays
  • Improved Essays

    Sickle cell crisis is an acute condition of sickle cell anemia. Sickle cell anemia is a genetic condition. Both parents must be carriers of the gene in order for a baby to be born with sickle cell anemia. In the United States, the gene predominantly affects black people of African decent. Sickle cell anemia is a disease where there is an inadequate number of healthy red blood cell throughout the body.…

    • 932 Words
    • 4 Pages
    Improved Essays
  • Improved Essays

    Sickle Cell Research Paper

    • 1038 Words
    • 5 Pages

    Scientist are continuing to prevail in finding treatments and they have been able to find new experimental treatments that can help reduce the pain of sickle cell anemia. These experimental treatments include gene therapy, nitric oxide, statins, and drugs to help boost fetal hemoglobin blood cell…

    • 1038 Words
    • 5 Pages
    Improved Essays
  • Improved Essays

    Sickle cell anemia is a genetic blood disorder that causes normal red blood cells to form into an irregular shape, called sickled-cells. The sickle cell gene causes the body to produce abnormal hemoglobin. After a while, the hemoglobin will then cluster together anywhere in the body causing the blockage of blood flow through the blood vessels. This blockage deprives the tissues and blood of oxygen which can lead to many difficulties and problems. SCD becomes life-threatening when the damaged red blood cells begin to breakdown, when the spleen does not work properly or at all, or when it is unable to prevent infections from coming in.…

    • 1506 Words
    • 7 Pages
    Improved Essays
  • Superior Essays

    Essay On Sickle Cell

    • 1260 Words
    • 6 Pages

    Hemoglobin job is to allow red blood cells to carry oxygen throughout the body. Abnormal hemoglobin causes the red blood cell to become rigid, sticky, and misshapen. The sickle cell gene can be referred to as Autosomal recessive inheritance, because it is passed down through generations in a pattern of inheritance. A child can be affected by sickle cell is the mother and father passes down a defective gene. If only one parent passes the sickle cell gene the child will have the trait; sickle cell trait produces both normal and sickle cell hemoglobin.…

    • 1260 Words
    • 6 Pages
    Superior Essays