Hemochromatosis Q. 1 MOST common mutation seen in heriditary hemochromatosis is: A C282Y B H63D C TFR2 D SLC11A3 Q. 1 MOST common mutation seen in heriditary hemochromatosis is: A C282Y B H63D C TFR2 D SLC11A3 Ans. A Explanation: The most common mutation in hereditary hemochromatos is a homozygous G to A mutation resulting […]
Hemochromatosis HEMOCHROMATOSIS Hemochromatosis is a common inherited disorder of iron metabolism leading to deposition of excessive amount of iron in parenchymal cells leading to fibrosis and organ failure. The iron storage pigment in tissues is called as hemosiderin (least in skin). Hemosiderosis is an acquired condition. Liver is the first organ to be affected &
