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Hereditary haemochromatosis: a tale of eight siblings

Shrikant D Pande1, Rajkumar Ariyaratnam, Michael J Burke

  • 1Changi General Hospital, Singapore. shrikantpande@yahoo.co.uk

Clinical Medicine (London, England)
|January 26, 2010
PubMed

Hereditary haemochromatosis (HH) is an autosomal recessive condition in which inappropriately excess iron absorption from the intestine results in pathological deposition of iron in the parenchymal cells of organs leading to tissue damage associated with characteristic arthropathy. It is an important cause of joint pain in middle age and early diagnosis and treatment can reduce the long-term complications of the disease.

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