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Canada's most common genetic disorder — 1 in 9 are carriers
Header Information
Did You Know...
1 in 9 Canadians carries the mutated gene for Hemochromatosis
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PDF Versions
Adobe PDF versions of hemochromatosis FAQs and information about the disorder are also available on this site:
Get the free Acrobat Reader by visiting the Adobe web site.
DNA Testing for Hereditary Hemochromatosis
Hereditary hemochromatosis is caused by defects in a gene called HFE. DNA testing can confirm the presence of the three mutations which are known to cause hemochromatosis: C282Y, H63D and S65C. DNA testing can be done to find out if your family may be at risk.
A confidential HFE genetic testing using buccal (mouth) swab collection is available through Genetrack Biolabs at www.hemochromatosisdna.com.
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The Disorder
The Canadian Hemochromatosis Society has developed detailed information about several aspects of the disorder, below. For a quick overview of hemochromatosis and the CHS, see the FAQs (frequently asked questions) section of this site.
What is It?
A thorough explanation of the disorder and the development of symptoms.
How Common is It?
A review of the hereditary complexity of hemochromatosis.
Symptoms
Symptomology of the disorder, and how to spot common signs of possible affliction.
Diagnosis / Testing
Information on who should be tested, as well as common testing methods.
Genetic Inheritance
Graphical representations of possible inheritance.
Treatment
Effective management of hemochromatosis and its effects.
Dietary Precautions
Information on iron intake and other dietary issues.
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