Hemochromatosis testing may involve multiple diagnostic procedures, such as radiography, blood tests, genetic testing, and liver biopsy. Learn more here.

Blood tests are one of the key ways to confirm a diagnosis of hemochromatosis. Additional testing might include an MRI, genetic testing, and a liver biopsy.

ANSWER: Hereditary hemochromatosis (HHC) is a genetic disease of iron overload. In a person with HHC, the intestines absorb as much iron as they can all the time, even if the body doesn’t need ...

Hereditary hemochromatosis is a genetic condition that causes the buildup of iron in your body. Learn about symptoms, causes, treatment, and more.

Nat Clin Pract Gastroenterol Hepatol. 2006;3(4):178-179. Although hemochromatosis was first described in the 19 th century, John Sheldon's 1934 description of 300 cases remains a landmark ...

Genetic testing is a type of medical testing process that is used to detect genetic mutations, or variations in your DNA, chromosomes, or proteins, that are associated with genetic disorders. It ...

After a genetic test, Alex Swanson learned he has hereditary hemochromatosis, a condition causing iron overload that can lead to severe health issues if untreated. Just $2 for 6 months! SUBSCRIBE NOW ...

The raison d'être behind genetic screening is that genotype predicts phenotype (disease risks). But it isn't always so. The likelihood of a specific mutation in the BRCA1 gene causing breast cancer, ...

Genetic testing for HFE mutations will confirm the diagnosis in over 90% of cases.” Treatment: Dr Rohan Badave concluded, “Phlebotomy is the standard treatment for primary hemochromatosis.

DEAR DR. ROACH: My husband was diagnosed with hemochromatosis 13 months before he died. I recommended that his blood relatives get tested so they can get treatment early, if necessary.