General Biology 1 Sickle cell anemia is an inherited disease in which there aren’t enough healthy red blood cells to carry oxygen throughout the body . Where the cell is deformed is in the bone marrow ‚a gene in the bone marrow causes the blood cell to come out in a sickle cell shape because the hemoglobin in the defected body is abnormal‚ after it gives up the oxygen‚ bet together causeing the red blood cells to become to a sickle like shape.People with Sickle cell anemia have abnormal hemoglobin
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Sickle cell anemia is a genetic disease that affects the shape and functionality of red blood cells. It is caused by a mutation in the DNA of the protein‚ hemoglobin‚ specifically in the beta chain. There are 531 base pairs in this DNA strand. Substitution or point mutation occurs‚ causing “GAG” to become “GTG”. This results in valine being created instead of glutamate. The mutation causes the hemoglobin to cling together in low oxygen levels and the red blood cell changes shape‚ preventing it from
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Abstract Transitional age youth between the ages of 15-18 who are battling chronic illnesses such as Sickle Cell Disease (SCD) traditionally have a hard time coping to their life style. This causes some to fall into depression and the outlook of the quality of life is decreased also. The eight week study will include six African- American boys and girls from an outpatient clinic that specializes in the medical care of persons with SCD. Participants will meet twice a week for an hour. The Children’s
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Sickle-cell disease‚ also known as sickle-cell anaemia‚ is a hereditary blood disorder‚ caused by an abnormality in the oxygen-carrying protein hemoglobin found in red blood cells. This leads to a propensity for the cells to assume an abnormal‚ rigid‚ sickle-like shape under certain circumstances. Sickle-cell disease is associated with a number of acute and chronic health problems‚ such as severe infections‚ attacks of severe pain‚ stroke‚ and an increased risk of death. Sickle-cell disease occurs
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Differential diagnose 1: Sickle Cell Anemia A 17-year-old African American female presented to the clinic with the following symptoms‚ chest and abdominal pain‚ and jaundice eyes. Her vital signs revealed B/P 98/50‚ pulse 112‚ respiration. 28 and temp. 99.9. EKG and chest x-ray completed with the result within normal range. She was discharged‚ and within four hours returned to the ER. Sickle cell disease is defined as a group of heredity disorder characterized by abnormal hemoglobin‚ called hemoglobin
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Sickle Cell Disease is an illness that affects people all across the globe. This paper will give a description of the sickness through the discussion of the causes‚ symptoms‚ and possible cures. Sickle Cell Disease (SCD) is a "group of inherited red blood cell disorders."(1) These disorders can have various afflictions‚ such as pain‚ damage and a low blood count--Sickle Cell Anemia. The overall incidence of SCD is eight out of 100‚000 people. However‚ it is much more widespread in some people.
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Critical Care Nursing: Sickle Cell Anemia Critical Care Nursing 10/15/2009 Sickle cell anemia affects millions of people worldwide. Sickle cell anemia is a disease in which your body produces abnormally shaped red blood cells. They don’t last as long as normal‚ round red blood cells‚ which leads to anemia. Sickle cells contain abnormal hemoglobin that causes the cells to have a sickle shape. Sickle-shaped cells don’t move easily through your blood vessels. They’re
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Cell’s July 18‚ 2011 Sickle cell anemia is an inherited blood disease that means you are born with it and it lasts a lifetime. People with sickle cell anemia inherit two variant or sickle cell genes‚ one from each parent. In the United States‚ sickle cell anemia affects about 72‚000 people. About 2 million Americans carry the sickle cell trait but about 1 in 12 African Americans have the trait. The signs and symptoms of sickle cell anemia are different in each person. Some people
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Sickle Cell Disease (SCD) is a group of inherited red blood cell disorders. People with Sickle Cell Disease have abnormal hemoglobin‚ called hemoglobin S or sickle hemoglobin‚ in their red blood cells. People with SCD inherit two abnormal hemoglobin genes‚ one from each of their parents. One of these abnormal hemoglobin genes causes the production of hemoglobin S in the body.1 When a person has two hemoglobin S genes‚ Hemoglobin SS‚ this disease is called Sickle Cell Anemia.1 This is the most common
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Sickle Cell Anemia is a hereditary disease that changes the smallest and most important components of the body. A gene causes the bone marrow in the body to make sickled shapes‚ when this happens; it causes the red blood cell to die faster. This is what causes Hemolytic Anemia. Older children and adults with sickle cell disease may experience a few complications‚ or have a pattern of ongoing problems that shorten their lives. The most common and serious complications of sickle cell disease are anemia
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