[Management of hyperferritinemia]

Rev Med Liege. 2006 May-Jun;61(5-6):329-33.
[Article in French]

Abstract

Hemochromatosis is the most common genetic disorder in persons of northern European descent, and the majority of cases are caused by a mutation in the gene HFE. Genetic testing for hemochromatosis is therefore indicated in all patients with increases in transferrine saturation and ferritin levels. When this genetic testing does not demonstrate a hemochromatosis, other diseases responsible for elevated ferritin levels have to be ruled out, mainly hemolytic anemia, chronic inflammatory disorders, liver diseases such as hepatitis B or C, alcohol abuse, and non alcoholic fatty liver disease. In demonstrated iron overload with absence of classic causes, second-line genetic testing should be considered.

Publication types

  • English Abstract
  • Review

MeSH terms

  • Algorithms
  • Ferritins / blood*
  • Hemochromatosis / blood
  • Hemochromatosis / complications
  • Hemochromatosis / diagnosis
  • Humans
  • Iron Metabolism Disorders / blood*
  • Iron Metabolism Disorders / complications
  • Iron Metabolism Disorders / diagnosis*
  • Iron Metabolism Disorders / genetics

Substances

  • Ferritins