juvenile hemochromatosis in iran: a case report with 5-year follow-up after treatment

نویسندگان

hossein nobakht

sheida zolfaghari

mohsen pourazizi

mojtaba malek

چکیده

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 fatty liver and was finally diagnosed as having juvenile hemochromatosis. a review of the scientific literature reveals that recently only three siblings suffering from the disease have been reported in iran.

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عنوان ژورنال:
middle east journal of digestive diseases

جلد ۸، شماره ۲، صفحات ۱۴۳-۰

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