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- W2147888917 abstract "Sickle cell disease (SCD) and thalassaemia major are the most important syndromes of the haemoglobinopathies. Complications of SCD can be life threatening and include stroke, hyposplenism and vaso-occlusive crises. Treatment of SCD is generally supportive or by transfusion, hydroxyurea or bone marrow transplant (BMT). β Thalassaemia major is treated with transfusion and chelation for the resulting iron overload which is the cause of most morbidity, with BMT the only curative procedure." @default.
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- W2147888917 date "2002-08-01" @default.
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- W2147888917 title "The management of haemoglobinopathies" @default.
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- W2147888917 doi "https://doi.org/10.1054/cupe.2002.0301" @default.
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