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Beta thalassemia syndromes: New insights

18 Dec 2024

Abstract excerpt

Beta thalassemia (β-thalassemia) syndromes are a heterogeneous group of inherited hemoglobinopathies caused by molecular defects in the beta-globin gene that lead to the impaired synthesis of beta-globin chains of the hemoglobin. The hallmarks of the disease include ineffective erythropoiesis, chronic hemolytic anemia, and iron overload. Clinical presentation ranges from asymptomatic carriers to severe anemia...

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PMID: 40191679
DOI: 10.12998/wjcc.v13.i10.100223

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