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The role of iron overload on oxidative stress in sickle cell anemia

✍ Scribed by dos Santos, Talyta Ellen de Jesus; de Sousa, Geane Félix; Barbosa, Maritza Cavalcante; Gonçalves, Romélia Pinheiro

Book ID
120081206
Publisher
Future Medicine
Year
2012
Tongue
English
Weight
571 KB
Volume
6
Category
Article
ISSN
1752-0363

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## Abstract Sickle cell disease (SCD) is a class of hemoglobinopathy in humans, which causes a disruption of the normal activities in different systems. Although this disease begins with the polymerization of red blood cells during its deoxygenating phase, it can erupt into a cascade of debilitatin