Llwytho...
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...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Middle East J Dig Dis |
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| Prif Awduron: | , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
Iranian Association of Gastroerterology and Hepatology
2016
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| Pynciau: | |
| Mynediad Ar-lein: | 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 |
| Tagiau: |
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