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03

Human Genetic Disorders ? Research Report

   
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Title: Human Genetic Disorders ? Research Report
 
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Subject: Science
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Date: September 11, 1999
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Length: 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)...
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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...
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