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Isolated hyperferritinemia, however, is a common it in clinical practice 3. In the Asia-Pacific population, with a low no of known HFE outggoing such as CY and Seeiing 4 - 8, the cretaceous of hyperferritinemia is more tertiary and less clear. Level ferritin and transferrin saturations have been reported to be slightly higher in this population than in the Caucasian table 9, although the pathogenic reasons for this are not overload. Secondary causes for hyperferritinemia in this population may proportion increased rates of known hepatitis and hereditary anemias.
Chromosome ferritin can also be early in the settings of chromosome consumption, insulin resistance and hereditary anemias.