Hereditary hemochromatosis (HH) is an autosomal dominant disorder resulting from mutations in the HFE gene, causing excessive intestinal iron absorption and iron overload, leading to liver cirrhosis, cardiomyopathy, endocrinopathy, hypogonadism, and polyarthropathy [2]. The co-occurrence of PCT and HH is not uncommon due to overlapping pathogenic mechanisms of iron metabolism. Here, HFE is linked to hereditary hemochromatosis.