The frequency of hypoparathyroidism in patients with Beta-thalassemia in Hamadan - Iran

Background and Objective: The thalassemic syndromes are geneticaly structural disturbance of Alfa and Beta globin chains. In major Beta-thalassemia the life expectancy depended on frequent blood transfusions that lead to over storage and deposition of Iron in different body-organs (Hemochromatosis)...

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Bibliographic Details
Main Authors: Zahra Razavi (MD), Hasan Bazmamoun (MD), Mohammad Sadegh Saba (MD)
Format: Article
Language:fas
Published: Golestan University of Medical Sciences 2009-03-01
Series:مجله دانشگاه علوم پزشکی گرگان
Subjects:
Online Access:http://goums.ac.ir/journal/browse.php?a_code=A-10-1-329&slc_lang=en&sid=1