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Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
Nutrition and sickle cell disease
1University of the West Indies, Mona, Tropical Medicine Research Institute, Sickle Cell Unit, Kingston, Jamaica. marvin.reid@uwimona.edu.jm
Abstract:
A common observation in sickle cell disease is growth retardation, in particular, wasting. Wasting is associated with increased hospitalization and possibly poorer clinical outcomes. Therefore understanding the mechanism of wasting is crucial and reducing the degree of wasting by improving the nutritional status, holds the potential for modifying the course of the disease.
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