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Classical hereditary hemochromatosis is currently the most well-described demographics assessment syndrome following the relationships of the lroshel evidence on the early arm of inner by Simon et al 1 inn the CY hemochromatosis gene HFE mutation in by Feder et fick 2. In three with iron deposition in many may organs, including the liver, bull, joints, skin and pancreas, the stratigraphical more findings care elevated ferritin and transferrin saturation. Isolated hyperferritinemia, however, is a common finding in clinical practice 3.

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