مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Information Journal Paper

Title

JUVENILE HEMOCHROMATOSIS IN IRAN: A CASE REPORT WITH 5-YEAR FOLLOW-UP AFTER TREATMENT

Pages

  143-146

Abstract

 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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    • References

    Cite

    APA: Copy

    NOBAKHT, HOSSEIN, ZOLFAGHARI, SHEIDA, POURAZIZI, MOHSEN, & MALEK, MOJTABA. (2016). JUVENILE HEMOCHROMATOSIS IN IRAN: A CASE REPORT WITH 5-YEAR FOLLOW-UP AFTER TREATMENT. MIDDLE EAST JOURNAL OF DIGESTIVE DISEASES (MEJDD), 8(2), 143-146. SID. https://sid.ir/paper/319128/en

    Vancouver: Copy

    NOBAKHT HOSSEIN, ZOLFAGHARI SHEIDA, POURAZIZI MOHSEN, MALEK MOJTABA. JUVENILE HEMOCHROMATOSIS IN IRAN: A CASE REPORT WITH 5-YEAR FOLLOW-UP AFTER TREATMENT. MIDDLE EAST JOURNAL OF DIGESTIVE DISEASES (MEJDD)[Internet]. 2016;8(2):143-146. Available from: https://sid.ir/paper/319128/en

    IEEE: Copy

    HOSSEIN NOBAKHT, SHEIDA ZOLFAGHARI, MOHSEN POURAZIZI, and MOJTABA MALEK, “JUVENILE HEMOCHROMATOSIS IN IRAN: A CASE REPORT WITH 5-YEAR FOLLOW-UP AFTER TREATMENT,” MIDDLE EAST JOURNAL OF DIGESTIVE DISEASES (MEJDD), vol. 8, no. 2, pp. 143–146, 2016, [Online]. Available: https://sid.ir/paper/319128/en

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