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Internal Medicine
Sickle cell disease (SCD) is an inherited hemoglobinopathy characterized by a mutation in the beta-globin gene, leading to the production of Hemoglobin S (HbS). This condition causes chronic hemolytic anemia and various complications, including pain crises and organ damage. The presentation outlines the prevalence of SCD, particularly among African and Hispanic populations, and emphasizes the importance of mental health support and comprehensive management strategies for affected individuals.
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