International consensus on the diagnosis and management of endocrine complications of β and α thalassemia in children and adolescents
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β-thalassemia (βT) and α-thalassemia (αT) are chronic hemolytic anemias caused by hereditary defects in the β or α chains of hemoglobin respectively. According to the clinical picture, both forms of thalassemia are subdivided into minor, intermedia or ma... ...
