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Medifocus Guidebook on:
Hereditary Hemochromatosis Updated: October 27, 2009
105 Pages LEARN MORE and download a FREE 25 page Preview of the Medifocus Guidebook on Hereditary Hemochromatosis |
Hereditary HemochromatosisHereditary hemochromatosis is an inherited, autosomal recessive disorder of iron metabolism that causes the body to absorb and store an excess amount of iron resulting in "iron overload" disease. If left untreated, hereditary hemochromatosis can result in the progressive accumulation of iron in the liver, pancreas, heart, joints, and pituitary gland leading to potentially serious complications including cirrhosis of the liver, diabetes, and heart problems. The good news is that early diagnosis and treatment can effectively reduce the body's iron overload, prevent organ damage, and enable patients to lead normal and productive lives. Surprisingly, many people have never heard about hereditary hemochromatosis even though it is one of the most common genetic disorders in the United States. It has been estimated that approximately 0.5% of the U.S. Caucasian population carry two copies of the defective gene (HFE gene) that is responsible for the disorder. Hereditary hemochromatosis is also the most commonly inherited liver disease in Europe. Signs and symptoms of hereditary hemochromatosis include generalized weakness and fatigue, joint pain, abdominal pain, and a bronze discoloration of the skin. Some patients may also have an enlarged liver or spleen. Diagnosis of hereditary hemochromatosis is based upon a thorough medical history, physical examination, and laboratory tests to measure for iron overload. If hereditary hemochromatosis is suspected, your doctor will order a genetic blood test to look for the HFE mutation that is responsible for the disorder. Early diagnosis and treatment of hereditary hemochromatosis is critical in order to prevent damage to vital organs and prevent serious complications such as cirrhosis of the liver and diabetes. The objectives of treatment are to remove excess iron from the body and prevent organ damage. Treatment consists of therapeutic phelebotomy which involves removing one unit of blood once a week until the iron levels have returned back to the normal range. Iron chelation therapy may be considered an option for patients who are not appropriate candidates for therapeutic phlebotomy. Learn more by ordering your MediFocus Guidebook on Hereditary Hemochromatosis, the most comprehensive, up-to-date source of information available. You will get answers to your questions, including:
You won't find this combination of information anywhere else. Your health matters. Don't leave it to chance. Arm yourself with the most comprehensive, up-to-date research available by ordering your MediFocus Guidebook today. Click here to preview the MediFocus Guidebook on Hereditary Hemochromatosis. |
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