Hemochromatosis

What is Hemochromatosis?

A disorder of iron metabolism characterized by excessive absorption of ingested iron, saturation of iron-binding protein, and deposition of hemosiderin in tissue, particularly in the liver, pancreas, and skin; cirrhosis of the liver, diabetes (bronze diabetes), bronze pigmentation of the skin, and, eventually heart failure may occur; also can result from administration of large amounts of iron orally, by injection, or in forms of blood transfusion therapy.

Questions and answers on "Hemochromatosis"

I've been tested for hemochromatosis. The result showed that I carry the H63D mutation. My previous blood work showed my iron, serum level of 190,...

doctor1 MD

Hello and welcome to HCM,

Hemochromatosis is a hereditary (autosomal recessive) condition caused by mutation of gene HFE. The most common mutation...

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I was diagnosed with hemochromatosis last year. Was a compound heterozygote with a family history of the diseases. Liver biopsy confirmed slight...

doctor1 MD

hi.
thanks for posting query at HCM

C282Y gene testing maybe done. mutation in this gene may confirm the clinical diagnosis of haemochromatosis in...

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If my husband has hemochromotosis and I am a carrier, should our children be tested for the HFE gene?

doctor1 MD

Brief Answer:
Hemochromatosis and genetics

Detailed Answer:
Thank you for contacting HCM with your health care concerns

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