Gastroenterology clinic

Screening, investigating and managing haemochromatosis

Jon Watson



Usually developing in patients aged between 30 and 60 years, haemochromatosis can lead to severe systemic complications if untreated. Here, Dr Watson outlines his approach to this condition.

Article Extract

  • Hereditary haemochromatosis is the most common inherited disease in Australia in people of Northern European descent. It is characterised by the deposition in various organs of excess iron (in the form of the iron-protein compound haemosiderin, formed by the polymerisation of ferritin). This leads to eventual fibrosis and functional organ failure.
  • Great advances have been made in recent years in our understanding of the genetics of hereditary haemochromatosis, and it is now recognised as a common phenotype resulting from mutations in at least five unique genes.