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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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Detalhes bibliográficos
Publicado no:Middle East J Dig Dis
Main Authors: Nobakht, Hossein, Zolfaghari, Sheida, Pourazizi, Mohsen, Malek, Mojtaba
Formato: Artigo
Idioma:Inglês
Publicado em: Iranian Association of Gastroerterology and Hepatology 2016
Assuntos:
Acesso em linha: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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