Anemia- a quantitative deficiency of the hemoglobin, often accompanied by a reduced number of red blood cells and causing pallor, weakness, and breathlessness.…
Anemia: is a condition where the body has a deficiency of healthy hemoglobin (red blood cells) to carry adequate oxygen to the tissues in the body.…
Read the case studies below and answer the questions that follow in two short essays that will be submitted as one deliverable.…
Anemia: A deficit in number and % of RBC’s and HgB usually from blood loss or extreme erythrocyte destruction and malformation. It causes dyspnea, pallor, palpitation, fatigue, and hypotension.…
The general presentation of anemia includes, but is not limited to: fatigue, dizziness, weakness, shortness of breath, pale color of skin, cold feet and hands, and irregular heartbeat. Our patient JJ, presents to the clinic two weeks postpartum for a well-baby visit, with complaints of being fatigued and having a “difficult time bouncing back from the delivery”. Though fatigue can be attributed to numerous disease states, JJ is at risk for developing anemia because she delivered her baby via caesarean section (C-section) and discontinued taking…
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…
1. Identify the etiologies and clinical manifestations common to all types of anemia. (See Table 42-1 p 870 and Chart 42-1 p 871)…
What are the functions of red blood cells? Name one blood cell disease and give a brief explanation the disease.…
A common form of anemia is iron deficiency anemia affecting many Americans today. Iron deficiency anemia is caused by the lack of iron in the body from diet. The lack of iron is also caused by growth spurts, pregnancy, and blood loss. (Family Doctor. Org, 2011) the problems with diet that people have are usually women and young children. Women that are pregnant or are nursing need a greater intake of iron. The iron deficiency form bleeding can occur during menstruation in women, ulcers of the stomach, and cancer.…
Furthermore, analyzing the association between genotype and phenotype could help in identifying genetic modifiers. Moreover, the whole genome sequencing project has many promising insights in terms of identifying and analyzing the genetic modifiers of sickle-cell disease (Steinberg et al., 2012). In this paper, we will investigate the main triggering factors of sickle-cell anemia, diagnostic process, and treatment…
Many people around the world die from different serious diseases such as cancers and blood diseases. One of severe blood diseases is pernicious anemia. Pernicious anemia starts from gastritis, atrophy of all stomach layers, and loss of normal gastric glands. [1] then develops to the deficiency in vitamin B12, and red blood cells (Erythrocytes). In the late stage, the patient will die; however, if the disease discovers early patient can do well in treatment. To clarify the stages of developing pernicious anemia, this essay will explain the changes that occur in the body in each step.…
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.…
INTRODUCTION: “Pain” sudden or chronic, lasting from a few hours to a few days; from a few weeks to a few months evolving from an adhesive substance in red blood cells. The “Pain” is inherited by an retriction blood flow through the body do to an abnormality in the cells. “Sickle Cell Anemia” a chronic illness discovered in 1910 by an American physician named James Bryan Herrick. Sickle Cell is more that just pain; it is a disease that is affected by abnormal blood cells that has an adhesive formation causing the natural flow to be compromised. As a result, these abnormal cells become fixed in the blood stream and not flowing to major body organs causing extreme pain and even a stroke. Why is this process painful? Have sickle cell patient become tolerant to pain or is it because some of them handle self-care management? For many years there has been a link between Sickle Cell Anemia and Pain caused by the stickiness of the blood cells. When this occurs, it decreases normal blood flow to the major organs causing strokes.(citation ). Sickle cell anemia is most common in people whose families come from Africa, South or Central America (especially Panama), Caribbean islands, Mediterranean countries (such as Turkey, Greece, and Italy), India, and Saudi Arabia. In the United States, it's estimated that sickle cell anemia affects 70,000–100,000 people, mainly African Americans. The disease occurs in about 1 out of every 500 African American births. Sickle cell anemia also affects Hispanic Americans. The disease occurs in more than 1 out of every 36,000 Hispanic American births (Citation).More than 2 million Americans have sickle cell trait. The condition occurs in about 1 in 12 African Americans. In people with sickle cell disease, approximately 50% do not survive beyond age 20 years, and most people do not live past 50 years of age (Citation)…
with the Sickle Cell disease, and based on these studies, the longevity and quality of life of these patients have greatly improved (Wethers, 2000). It has been researched and proven that Sickle Cell Anemia…
In sickle cell anemia, the number of red blood cells is low because sickle cells don't last very long. Sickle cells usually die after only about 10 to 20 days. The bone marrow can't make new red blood cells fast enough to replace the dying ones.…