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MRI Evaluation of Liver Iron Concentration in Patients with β-Thalassemia Major
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نویسنده
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Karimi Mehran ,Emad Marvasti Vahid ,Rasekhi Alireza ,Kumar Perikala Vigayananda ,Bordbar Mohammadreza ,Moshiri Alireza ,Hasanpour Peyman ,Serajzadeh Kazem
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منبع
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hepatitis monthly - 2010 - دوره : 10 - شماره : 2 - صفحه:149 -150
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چکیده
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Β-thalassemia major is a hereditary anemia, characterized by a genetic deficiency in the synthesis of the β-globin chain (1). the main complication of the multiple blood transfusions to these patients is iron overload and the deposition of iron in various organs, such as the reticuloendothelial system, the liver, the heart and the endocrine glands (2).
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آدرس
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shiraz university of medical sciences, Nemazee Hospital, Hematology Research Center, ایران, shiraz university of medical sciences, Nemazee Hospital, Hematology Research Center, ایران, shiraz university of medical sciences, Department of Radiology, ایران, shiraz university of medical sciences, Department of Pathology, ایران, shiraz university of medical sciences, Nemazee Hospital, Hematology Research Center, ایران, shiraz university of medical sciences, Nemazee Hospital, Hematology Research Center, ایران, shiraz university of medical sciences, Nemazee Hospital, Hematology Research Center, ایران, shiraz university of medical sciences, Nemazee Hospital, Hematology Research Center, ایران
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پست الکترونیکی
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karimim@sums.ac.ir
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Authors
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