Hemochromatosis in a β-thalassemia minor patient with H63D homozygous
mutation: A case report
Abstract
We report the case of a 73-year-old man who was presumed to have iron
deficiency anemia and was treated with iron supplements since
adolescence. His workup revealed β-thalassemia minor and H63D homozygous
hereditary hemochromatosis complicated with liver cirrhosis and
hepatocellular carcinoma.