Literature DB >> 25064705

Iron-refractory iron deficiency anemia (IRIDA).

Matthew M Heeney1, Karin E Finberg2.   

Abstract

Iron deficiency anemia is a common global problem whose etiology is typically attributed to acquired inadequate dietary intake and/or chronic blood loss. However, in several kindreds multiple family members are affected with iron deficiency anemia that is unresponsive to oral iron supplementation and only partially responsive to parenteral iron therapy. The discovery that many of these cases harbor mutations in the TMPRSS6 gene led to the recognition that they represent a single clinical entity: iron-refractory iron deficiency anemia (IRIDA). This article reviews clinical features of IRIDA, recent genetic studies, and insights this disorder provides into the regulation of systemic iron homeostasis.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Hepcidin; Inherited iron deficiency; Iron-refractory iron deficiency anemia; Matriptase-2; TMPRSS6

Mesh:

Year:  2014        PMID: 25064705     DOI: 10.1016/j.hoc.2014.04.009

Source DB:  PubMed          Journal:  Hematol Oncol Clin North Am        ISSN: 0889-8588            Impact factor:   3.722


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