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Iron Metabolism in Thalassemia and Sickle Cell Disease.
There are two main mechanisms by which iron overload develops in thalassemias: increased iron absorption due to ineffective erythropoiesis and blood transfusions. In nontransfused patients with severe thalassemia, abnormal dietary iron absorption increases body iron burden between 2 and 5 g per year...
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| Asıl Yazarlar: | , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Università Cattolica del Sacro Cuore
2009
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3033158/ https://ncbi.nlm.nih.gov/pubmed/21415988 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4084/MJHID.2009.006 |
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