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:

دوره 8  شماره 

صفحات  -

تاریخ انتشار 2016