Heba Abolaban, Munes Fares, Qusay Haydour, Nazir Ibrahim, Dona Rayess, Maria Diab, Ahmad M Al Moujahed

2010

Cochrane Database of Systematic Reviews

11

John Wiley & Sons, Ltd

Our site uses cookies to improve your experience. You can find out more about our use of cookies in About Cookies, including instructions on how to turn off cookies if you wish to do so. By continuing to browse this site you agree to us using cookies as described in About Cookies … Your language preference is set to English. Where translations are available, article sections will display in this language. Return to English … To assess the benefits and harms of TEA versus phlebotomy in the treatment of hereditary haemochromatosis … Hereditary haemochromatosis is an autosomal recessive disorder characterised by increased iron absorption and deposition in tissues (Hanson 2001). It is one of the most common inherited disease in Europeans (Bathum 2001), with a prevalence of nearly one in every 300 individuals (Powell 2002) … A mutation in the high iron Fe (HFE) gene (haemochromatosis gene on the short arm of chromosome 6) has been identified to …