| Literature DB >> 25064705 |
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.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