Copyright
©The Author(s) 2016.
World J Hepatol. Mar 18, 2016; 8(8): 395-400
Published online Mar 18, 2016. doi: 10.4254/wjh.v8.i8.395
Published online Mar 18, 2016. doi: 10.4254/wjh.v8.i8.395
Table 1 Classification of iron overload and hemochromatosis
Genetic iron overload (primary) |
Type 1 HFE-associated hemochromatosis |
C282Y homoyzygosity |
C282Y/H63D compound heterozygosity |
Type 2 juvenile hemochromatosis |
2A hemojuvelin mutations |
2B hepcidin mutations |
Type 3 TfR2-related hemochromatosis |
Transferrin receptor 2 |
Type 4 ferroportin disease |
Loss of function mutations, also called type 4A or "M" |
Hepcidin resistance mutations, also called type 4B or "H" |
Aceruloplasminemia |
Ceruloplasmin mutations |
A(hypo)transferrinemia |
Acquired iron overload (secondary) |
Ineffective erythropoiesis |
Thalassemia major |
Sideroblastic anemia |
Chronic hemolytic anemia |
Dietary iron overload (African) |
Parenteral iron overload (including transfusional overload) |
- Citation: Sivakumar M, Powell LW. Management of human factors engineering-associated hemochromatosis: A 2015 update. World J Hepatol 2016; 8(8): 395-400
- URL: https://www.wjgnet.com/1948-5182/full/v8/i8/395.htm
- DOI: https://dx.doi.org/10.4254/wjh.v8.i8.395