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Hemochromatosis(Hereditary Hemochromatosis [HH]; Primary Hemochromatosis; Familial Hemochromatosis; Secondary Hemochromatosis)How to Say It: He-moe-chrome-uh-toe-sis
by
Amy Scholten, MPH DefinitionHemochromatosis is a disorder where iron builds up in the body. Early treatment can improve outcomes. There are two types:
CausesHereditary hemochromatosis is caused by a faulty gene that is passed from parents to children. The secondary type may be caused by:
Risk FactorsThings that may raise the risk of HH are:
Things that may raise the risk of the secondary type are:
SymptomsMost people do not have symptoms. Those who do may have:
DiagnosisThe doctor will ask about your symptoms and health history. A physical exam will be done. Blood tests will be done to check iron levels. This is enough to make the diagnosis. More tests may be done to look for a cause. TreatmentThe goal of treatment is to lower iron levels. Choices are:
PreventionHH cannot be prevented. The secondary type may be prevented. It depends on the cause. RESOURCES:American Hemochromatosis Society http://www.americanhs.org American Society of Hematology http://www.hematology.org References:Hemochromatosis. American Liver Foundation website. Available at: https://liverfoundation.org/for-patients/about-the-liver/diseases-of-the-liver/hemochromatosis. Accessed Jamuary 12, 2021.
Hemochromatosis. EBSCO DynaMed website. Available at: https://www.dynamed.com/condition/hemochromatosis.
Accessed January 12, 2021.
Hemochromatosis. National Institute of Diabetes and Digestive and Kidney Diseases website. Available at: ...(Click grey area to select URL) Accessed January 12, 2021. Pilling L, Tamosauskaite J. Common conditions associated with hereditary haemochromatosis genetic variants: cohort study in UK Biobank
BMJ 2019; 364. Last reviewed February 2020 by
EBSCO Medical Review Board
Marcin Chwistek, MD Last Updated: 1/12/2021 | |