Sickle-Cell Disease College Essays Samples For Students

Child and adolescent health issues require extra concentration due to the fact that an early disease can lead to an improper growth which may impact the entire life of a person and therefore it is important to ensure that childhood and adolescence diseases are looked after with extreme care in order to improve the quality of life and the growth of the patients. Sickle cell anemia is one of the widely studied subjects today, considering that it can cause acute chronic conditions which include severe pain and organ dysfunctional ties and has a high fatality rate. This disease is also known ...

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The research review, developed by Lanzkron, Wilson, Beach, Haywood, Park and Segal (2008), is dedicated to studying published literature on the efficacy, effectiveness and toxicity of hydroxyurea, when used in adults with sickle cell disease. Sickle stem disease is a dangerous condition that tends to decrease life expectancy by 25-30 years and cause high morbidity level, while hydroxyurea remains the only approved disease-modifying therapy (Lanzkron et al., 2008, p.939). Taking into account severity of the disease and the fact that the drug under study is the only available non-supportive therapy, studying its efficiency, efficacy and toxicity is highly relevant for ...

Sickle cell is a hereditary disease that that has no cure. The disease cause blood disorders and is the most common form of sickle cell disease. The disease affects the hemoglobin in the red blood cell since the disease cause mutation of hemoglobin (Genetics Home Reference 2012). Thus, an individual with the disease produce both normal and abnormal hemoglobin. The sickly abnormal cells block the blood flow. Hence, as the result of blocked blood flow in the body that the cause inflexibility of red blood cells can raise the risk for infection that are life threatening chronic diseases that can ...

Sickle cell anemia is an inherited disorder of the blood where the red blood cells form an abnormal crescent shape. The Red blood cells deliver oxygen from the lungs to the body tissues are generally flexible and round, facilitating them to move easily through the blood vessels. Nevertheless, in individuals with sickle cell anemia, the texture and shape of the red blood cells can vary. They turn out to be sticky, hard and take the shape of a disc. The cells die prematurely, resulting to a deficiency of red blood cells (David, 2011).
Sickle cell anemia is passed through families ...

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Sickle-cell anemia is a genetic blood disorder, which affects the red blood cells. It was first described in the medical literature in 1846. In 1910, Ernest Irons became first to write about the pathologically altered red blood cells of the patient with sickle-cell anemia (Serjeant 425-429). It is caused by the mutation of the gene encoding the synthesis of the hemoglobin. As a result, the hemoglobin of the affected people is defective (hemoglobin S). Glutamic acid in it is substituted with valine in the sixth position of the β-chain. This change greatly reduces the solubility of hemoglobin in ...

Sickle cell anemia is the most widely inherited genetic disorder in the United States. Folic acids are one important nutrient that helps increase and produce some red blood cells in the bone marrow. This paper investigates how folic acid has used a supplement for pregnant women.
Sickle cell anemia can be genetically passed to the baby from a mother who has it or who is a carrier. Symptoms of the disease include headaches, irritability, fatigue, dizziness, diarrhea, cold feeling, difficulty when breathing, difficulty concentrating and pale skin ( Lindenbaum, John, and Klipstein ,16 ).
Malnutrition in pregnant women is the commonest ...