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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
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)