[Detection of hereditary hemochromatosis]
- PMID: 17918491
[Detection of hereditary hemochromatosis]
Abstract
Hereditary hemochromatosis is one of the most common genetic disorders. The prognosis of hemochromatosis is normal when phlebotomy therapy is started prior to manifestation of cirrhosis or diabetes. High ferritin is not always a marker of iron overload and ferritin must thus be coupled with transferrin saturation. Only high transferrin saturation entails a genetic research (HFE or type 1). The identification of rare types of hemochromatosis (types 2-4) is only required in particular cases. The evaluation of the iron overload is now based on hepatic MRI determination rather than liver biopsy.
Similar articles
-
[Hemochromatosis--from an underdiagnosed curiosity to a common disease].Tidsskr Nor Laegeforen. 2009 Apr 30;129(9):863-6. doi: 10.4045/tidsskr.08.0084. Tidsskr Nor Laegeforen. 2009. PMID: 19415085 Review. Norwegian.
-
Genetic screening for HFE hemochromatosis in 6,020 Danish men: penetrance of C282Y, H63D, and S65C variants.Ann Hematol. 2009 Aug;88(8):775-84. doi: 10.1007/s00277-008-0679-1. Epub 2009 Jan 22. Ann Hematol. 2009. PMID: 19159930
-
[Diagnosis and treatment of primary hemochromatosis].Ned Tijdschr Geneeskd. 1999 Jul 3;143(27):1404-8. Ned Tijdschr Geneeskd. 1999. PMID: 10422553 Review. Dutch.
-
Hereditary hemochromatosis. Detecting and correcting iron overload.Postgrad Med. 1994 Oct;96(5):151-8, 161, 165. Postgrad Med. 1994. PMID: 7937414 Review.
-
Screening for hemochromatosis in asymptomatic subjects with or without a family history.Arch Intern Med. 2006 Feb 13;166(3):294-301. doi: 10.1001/archinte.166.3.294. Arch Intern Med. 2006. PMID: 16476869
Publication types
MeSH terms
LinkOut - more resources
Medical