Hemochromatosis : Articles

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Hemochromatosis is a disorder that interferes with iron metabolism, which results in too much iron in the body.
Source:ADAM
Date:September 22, 2006
Hemochromatosis is an inherited blood disorder that causes the body to retain excessive amounts of iron. This iron overload can lead to serious health consequences, most notably cirrhosis of the liver.
Source:Gale Encyclopedia of Medicine
Iron is a vital component of heme, the component of hemoglobin that transports oxygen in the blood. Iron deficiency is the world ' s most common cause of anemia (blood with low hemoglobin and red blood cell components).
Source:Gale Encyclopedia of Public Health
Iron is a mineral that the human body uses to produce the red blood cells (hemoglobin) that carry oxygen throughout the body. It is also stored in myoglobin, an oxygen-carrying protein in the muscles that fuels cell growth.
Source:Gale Encyclopedia of Alternative Medicine
Iron tests are a group of blood tests that are done to evaluate the iron level in blood serum, the body ' s capacity to absorb iron, and the amount of iron actually stored in the body. Iron is an essential trace element; it is necessary for the formation of red blood cells and certain enzymes.
Source:Gale Encyclopedia of Medicine
Iron tests consist of four assays performed on serum or plasma to aid in the diagnosis and treatment of iron deficiency or iron overload. These tests are serum iron, total iron binding capacity (TIBC), serum ferritin, and serum transferrin.
Source:Gale Encyclopedia of Nursing and Allied Health
Hemochromatosis is an inherited blood disorder that causes the body to retain excessive amounts of iron. This iron overload can lead to serious health consequences, most notably cirrhosis of the liver.
Source:Gale Encyclopedia of Genetic Disorders Part I
Hemochromatosis is an inherited blood disorder that causes the body to retain excessive amounts of iron. This iron overload can lead to serious health consequences, most notably cirrhosis of the liver.
Source:Gale Encyclopedia of Genetic Disorders Part II
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