Sickle cell anemia thesis

Normal red blood cells are rounded and disk-shaped. In sickle cell anemia, some red blood cells become deformed, so they look like sickles used to cut wheat. These unusually shaped cells give the disease its name. Sickle cell anemia is one of a group of disorders known as sickle cell disease. Sickle cell anemia is an inherited red blood cell disorder in which there aren't enough healthy red blood cells to carry oxygen throughout your body.
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This disease causes reduced oxygen carrying capacity of RBC resulting in painful crisis, hemolytic anemia, and infection susceptibility. SCD affected individuals have high mortality rates. Early detection and constant monitoring of this disease is essential. The following review focuses on various methodologies that have emerged in the diagnosis of SCD. Also, low cost methods that can be easily adopted in developing nations are discussed.
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Normally a person has flexible and round blood cells. With Sickle Cell anemia, Hemoglobin molecules in red blood cells, that carry oxygen in the body. Case:- Doctor informed complete studies of a 9-year old child with sickle cell anemia. Her main complaints were cough, vague pains in legs joints , night sweats, abdominal pain, less hunger, and increasing weakness.
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We use cookies to give you the best experience possible. The tissues that do not receive enough blood flow are destroyed hence causing the sickle cell disease. Sickle cell anemia arises when the sickle cells are destroyed rapidly in the body of the people with the disease. Wang, 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. Genetically, sickle cell trait AS arises when there is both the production of both the hemoglobin A and S in the red blood cells hence having more A than S.
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