Asian forms of sickle cell
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The body subsequently becomes dehydrated, or with a fever. Even in the case of adequate medical care, severe disability or death may result in childhood and early adult years. They are present in Africa, S. This variation is similar to sickle cell-C disease except that an element has been replaced in the hemoglobin molecule. Infants and young children are at risk for life-threatening infections. Drinking plenty of water daily eight to 10 glasses or receiving fluid intravenously to prevent and treat pain crises.
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Adult Sickle Cell Disease Symptoms
Infection is the major cause of death in children younger than age 5 in this population. The decrease in red blood cells causes anemia. This variation is most often also seen in Southeast Asia populations. Any and all major organs are affected by sickle cell disease.
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Sickle cell disease in north carolina
Sickle cell HbSS is a genetic disease. Mild anemia may occur and red cells tend to be small. Any interruption in the flow of blood and oxygen to the brain can result in devastating neurological impairment. Specific treatment for sickle cell disease and its complications will be determined by your child's doctor based on.. The disease process results in severe anemia, oxygen deprivation, poor circulation and extreme pain. Sickle cell disease is an inherited blood disorder characterized by defective hemoglobin a protein in red blood cells that carries oxygen to the tissues of the body. These are also called vaso-occlusive crises.
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