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NORD is very grateful to Pauline Lee, PhD, Associate Professor of Molecular Medicine, The Scripps Research Institute, Department of Molecular and Experimental Medicine, for assistance in the preparation of this report.
Synonyms of Juvenile Hemochromatosis
- hereditary hemochromatosis type 2
- juvenile hereditary hemochromatosis
- type 2 hereditary hemochromatosis
- juvenile hemochromatosis type 2A
- juvenile hemochromatosis type 2B
Juvenile hemochromatosis is a rare genetic disorder characterized by the accumulation of iron in various organs of the body. Symptoms usually become apparent before the age of 30. The specific symptoms and severity of juvenile hemochromatosis vary from one person to another. Common symptoms include absent or decreased function of the testes in males or ovaries in females (hypotrophic hypogonadism), heart (cardiac) disease, scarring of the liver (cirrhosis), joint disease, diabetes, and dark discoloration of patches of skin (hyperpigmentation). These symptoms are similar to those seen in classic hereditary hemochromatosis. However, the symptoms associated with juvenile hemochromatosis occur at an early age and are usually more severe. If untreated, juvenile hemochromatosis can potentially cause life-threatening complications. Juvenile hemochromatosis is caused by mutations of one of at least two genes (the HJV and HAMP genes). These mutations are inherited as an autosomal recessive trait.
Juvenile hemochromatosis is classified as an iron overload disorder. It is a separate, distinct disorder from classic hereditary hemochromatosis. Juvenile hemochromatosis is caused by mutations to different genes and generally has an earlier age of onset and more severe iron accumulation.
Organizations related to Juvenile Hemochromatosis
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