| Literature DB >> 15331258 |
Anne L Matthews1, Sarah J Grimes, Georgia L Wiesner, Louise S Acheson.
Abstract
One of the most common genetic causes of iron overload is hereditary hemochromatosis (HHC), a condition characterized by overabsorption of dietary iron from the gastrointestinal tract. This condition can lead to excessive iron accumulation with resulting dysfunction in multiple organs, including the liver, skin, heart,joints, pancreas, and testes. The clinical consequences of HHC if undetected and untreated can be severe and include liver cirrhosis,hepatocellular carcinoma, diabetes mellitus, cardiac arrhythmias and failure, arthritis, and hypogonadism. HHC is one of the most common heritable conditions in white populations of Northern European origin. This article presents a case study of HHC, describing inheritance and genetics, disease characteristics and natural history, diagnosis, differential diagnosis, and management.Entities:
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Year: 2004 PMID: 15331258 DOI: 10.1016/j.pop.2004.04.007
Source DB: PubMed Journal: Prim Care ISSN: 0095-4543 Impact factor: 2.907