Hemochromatosis in a β‐thalassemia minor patient with H63D homozygous mutation: A case report

Abstract

Abstract β‐thalassemia heterozygosity can cause significant iron overload when accompanied by HFE gene mutations and inappropriate iron supplementation.

Keywords

• anemia
• h63d mutation
• hereditary hemochromatosis
• HFE gene
• iron overload
• β‐thalassemia