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Title: Human Genetic Disorders ? Research Report
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Science |
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| Date: |
September 11, 1999 |
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2 / 550 |
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Even if an individual has both copies of the abnormal gene the risk of actual clinical haemochromatosis is low (between 1-25%). Some other genes that cause haemochromatosis are the autosomal dominant SLC11A3/ferroportin 1 gene and TfR2 (transferrin receptor 2)... Showed first 250 characters
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They are much rarer than HFE-haemochromatosis.
For treatment of the disorder, a phlebotomy is most likely in order. Approximately one pint of blood is taken out of your system weekly, to reduce the increased iron levels. It may take a few months to a few years of weekly phlebotomy for an individual's system to have normal iron levels... Showed next 250 characters
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