©2007 Baishideng Publishing Group Co.
World J Gastroenterol. Sep 21, 2007; 13(35): 4673-4689
Published online Sep 21, 2007. doi: 10.3748/wjg.v13.i35.4673
Published online Sep 21, 2007. doi: 10.3748/wjg.v13.i35.4673
Table 1 Nomenclature for iron overload states
| Primary iron overload-hereditary haemochromatosis (HH) |
| HFE-associated HH |
| 1 C282Y homozygosity |
| 2 C282Y/H63D compound heterozygosity |
| 3 Other mutations |
| Non HFE-associated HH |
| 1 Juvenile haemochromatosis |
| 2 TfR2-related haemochromatosis |
| 3 Autosomal dominant haemochromatosis |
| Secondary iron overload-acquired |
| Iron-loading anaemias |
| 1 Thalassaemia major |
| 2 Sideroblastic anaemia |
| 3 Chronic haemolytic anaemias |
| Chronic liver diseases |
| 1 Hepatitis C |
| 2 Alcoholic liver disease |
| 3 Non-alcoholic steatohepatitis |
| 4 Porphyria cutanea tarda |
| 5 IR-HIO |
| 6 Post-portacaval shunting |
| 7 Transfusional and parenteral iron overload |
| 8 Dietary iron overload |
| Miscellaneous |
| 1 Iron overload in sub-Saharan Africa |
| 2 Neonatal iron overload |
| 3 Acaeruloplasminaemia |
| 4 Congenital atransferritinaemia |
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Citation: Sebastiani G, Walker AP.
HFE gene in primary and secondary hepatic iron overload. World J Gastroenterol 2007; 13(35): 4673-4689 - URL: https://www.wjgnet.com/1007-9327/full/v13/i35/4673.htm
- DOI: https://dx.doi.org/10.3748/wjg.v13.i35.4673