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Is the Role of Hepcidin and Erythroferrone in the Pathogenesis of Beta Thalassemia the Key to Developing Novel Treatment Strategies?

Thalassemia is a disease of erythrocytes that varies largely on its genetic composition and associated clinical presentation. Though some patients may remain asymptomatic, those with a complicated course may experience severe anemia early in childhood, carrying into adulthood and requiring recurrent...

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Principais autores: Tsz Yuen Au, Shamiram Benjamin, Oskar Wojciech Wiśniewski
פורמט: Artigo
שפה:Inglês
יצא לאור: MDPI AG 2022-09-01
סדרה:Thalassemia Reports
נושאים:
beta thalassemia
erythroferrone
<i>HAMP</i> polymorphisms
hepcidin
hemochromatosis
iron homeostasis
גישה מקוונת:https://www.mdpi.com/2039-4365/12/3/17
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