A paradigm shift on beta-thalassaemia treatment: How will we manage this old disease with new therapies?

© 2018 The Authors Beta-thalassaemia causes defective haemoglobin synthesis leading to ineffective erythropoiesis, chronic haemolytic anaemia, and subsequent clinical complications. Blood transfusion and iron chelation allow long-term disease control, and haematopoietic stem cell transplantation off...

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Bibliographic Details
Main Authors: Maria Domenica Cappellini, John B. Porter, Vip Viprakasit, Ali T. Taher
Other Authors: American University of Beirut Medical Center
Format: Review
Published: 2019
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/46572
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Institution: Mahidol University