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Changing patterns in the epidemiology of β‐thalassemia
β‐thalassemia major is an inherited hemoglobinopathy that requires lifelong red blood cell transfusions and iron chelation therapy to prevent complications due to iron overload. Traditionally, β‐thalassemia has been more common in certain regions of the world such as the Mediterranean, Middle East,...
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| Publicado no: | Eur J Haematol |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7692954/ https://ncbi.nlm.nih.gov/pubmed/32886826 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/ejh.13512 |
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