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Haemochromatosis Scholarly Peer-review Journal|OMICS International|Hereditary Genetics: Current Research

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Haemochromatosis Scholarly Peer-review Journal

Haemochromatosis is a genetic (inherited) disorder causing the body to absorb too much iron from the diet. The excess iron is then stored in various organs, mainly the liver.Haemochromatosis is an inherited condition caused by a faulty gene called HFE, which allows a person to absorb too much iron from food. Normally, the body only absorbs as much as it needs. The excess iron may also be stored in the pancreas, heart, testes/ovaries, skin and joints. The main treatment is the regular removal of blood, which helps to remove the excess iron from the body. If treatment is started early enough and before complications occur then the outlook for people with hemochromatosis is very good. The diagnosis includes blood test, Liver biopsy, and heart scan.Treatment is lifelong. It involves having blood taken out of the body, just like being a blood donor. Scholarly peer review is the process of subjecting an author'sscholarlywork, research, or ideas to the scrutiny of others who are experts in the same field, before a paper describing this work is published in a journal. The work may be accepted, considered acceptable with revisions, or rejected. Peer review requires a community of experts in a given (narrowly defined) field, who are qualified and able to perform reasonably impartial review. OMICS Group is a scientific organization and online publishing house that drives the progress of research through freely available open access journals and international conferences. With 700+ peer-reviewed journals in its list and many expert reviewers and scientists in its editorial board OMICS Group is among the best open access publishers of the world. Also, OMICS Group organizes more than 3000+ International Scientific Conferences annually and provides eBooks, and additional services such as ScholarsCentral. OMICS Group has got support of more than 1000+ Scientific associations, 50,000+ editorial board members and 15 million readers.
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Last date updated on March, 2024

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