Iron-refractory iron deficiency anemia (IRIDA)

Hematol Oncol Clin North Am. 2014 Aug;28(4):637-52, v. doi: 10.1016/j.hoc.2014.04.009. Epub 2014 May 28.

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.

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

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Anemia, Iron-Deficiency / diagnosis*
  • Anemia, Iron-Deficiency / genetics
  • Anemia, Iron-Deficiency / therapy*
  • Diagnosis, Differential
  • Humans

Supplementary concepts

  • Iron-Refractory Iron Deficiency Anemia