Hyperhemolysis Syndrome In A Patient With Sickle Cell Disease With Erythrophagocytosis In Peripheral Blood
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This review aims to highlight the importance of
Win N. (2009) Hyperhaemolysis syndrome in sickle cell disease. Expert Rev. Hematol. 2(2), 111-115. the patient's RBC reduction can lead to the activation of macrophages leading to peripheral
Hyperhemolysis syndrome in sickle cell disease
Hyperhemolysis syndrome in sickle cell disease (2009) Hyperhemolysis syndrome is a serious and potentially HbA and HbS levels in the peripheral blood as a marker to docu-