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Juvenile Hemochromatosis in Iran: A Case Report with 5-Year Follow-up after Treatment
Juvenile hemochromatosis is a rare autosomal recessive disorder that typically occurs in the first to third decades of life. Its symptoms are more acute and severe than classic hemochromatosis. We describe a 27-year-old man who was referred to the gastrointestinal clinic with a probable diagnosis of...
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| Publicat a: | Middle East J Dig Dis |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Iranian Association of Gastroerterology and Hepatology
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4885614/ https://ncbi.nlm.nih.gov/pubmed/27252822 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15171/mejdd.2016.20 |
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