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The Cause Of Sickle Cell Anemia Biology Essay. SDC in an inherited disease. It can be categorized into two types know as heterozygous sickle anemia and homozygous sickle anemia. A person receive one sickle cell disease gene from one parents and a normal gene from another parent, he will have a condition know as Sickle Cell Trait.
Sickle cell anemia is a hereditary disorder that affects countries that were previously affected by malaria - mostly the African Americans and Hispanic Americans (Newland, 2013). The people suffering from this disorder have in the past had barriers to access vital health information and care since it was not covered by the affordable act.
In Sickle Cell Anemia, the regular hemoglobin is mutated and changes from the normal hemoglobin A to hemoglobin S. the ability for a protein to be mutated that is located on the red blood cells means that this mutation can will be passed down to the person’s child, making this disease hereditary.
Sickle Cell Anemia is a disease in which someone carries abnormal hemoglobin (Hemoglobin S). Hemoglobin is a protein in red blood cells responsible for carrying oxygen throughout the body, however when people produce Hemoglobin S, it causes the red blood cells to distort into a crescent shape and become fragile, this interrupts healthy blood flow and leads to anemia.
Sickle cell anemia arises when the sickle cells are destroyed rapidly in the body of the people with the disease. (Wang, 2004) When the flow of blood is blocked to pass through the vessels the following condition arises; acute chest syndrome, pain episodes (arms, chest, legs, abdomen), prolonged erections that are painful, and organs like the kidney, spleen, and liver are damaged.
Further information can be found in literature, and on the websites of organizations such as the National Institutes of Health (NIH), the American Sickle Cell Anemia Association (ASCAA), the American Society of Hematology, the National Heart, Lung, and Blood Institute (NHLB), and many other groups.
Sickle cell anemia is an inherited disease in which the body is unable to produce normal hemoglobin, an iron-containing protein. Abnormal hemoglobin can morph cells that can become lodged in narrow blood vessels, blocking oxygen from reaching organs and tissues.
Sickle Cell Anemia Sickle Cell Anemia occurs in about 1 out of 500 African American births, and 1 out of 36,000 Hispanic births. It is a lifelong disease, and sometime can be deadly. According to Dr. Whittaker, in our region there are abnormally higher cases of Sickle Cell Anemia, so I found it important to learn more about the disease, what cause it, what are the symptoms as well as the.
Sickle cell anemia is caused by inherited genes, where people with the disease are born with two abnormal genes of the sickle cell, one from each parent. However, if the person is born with one normal gene and one sickle cell gene, will have a condition called sickle cell trait, meaning that he won’t have the disease but may have the chance to pass it on to his children (Sickle cell disease).
Symptoms of sickle cell disease include: irregular blood pressure, jaundice skin or eyes, pale skin, bone or joint pain, delayed growth, skin ulcers (common on the legs), anemia, constant headaches, dizziness, fatigue, organ or tissue damage, pulmonary hypertension, shortness of breath, numbness in the extremities, and stroke.
Sickle cell anemia refers to a blood disorder that is inherited and mainly affects the red blood cells of a person (Bjorklund 12). The normal red blood cells are round and they transport oxygen to all parts of the body through the small blood vessels.
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Sickle cell anemia is a disease in which the body produces abnormally shaped red blood cells that have a crescent or sickle shape. These cells do not last as long as normal, round, red blood cells, which leads to anemia (low number of red blood cells). The sickle cells also get stuck in blood vessels, blocking blood flow. Signs and symptoms of sickle cell disease usually begin in early.
Essay Instructions: please include what sickle cell is and a history of sickle cell with important dates and pioneers in research. talk about genetics and sickle cell. all so include races affected, geographical locations affected, how to test for sickle cell, signs and symptoms produced by sickle cell, how it affects the various body systoms (cardio, respritoy, ect.), treatment for it l ong.
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