Correction of dentofacial deformity in a thalassemic patient with orthognathic surgery: A case report

Introduction: Thalassemia is a genetically determined disorder of hemoglobin syntheses which results in problematic erythropoisis and finally leads to compensative dilation of bone marrow spaces and associated multiple skeletal disorders. These patients routinely are under hyper transfusion and in s...

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Bibliographic Details
Main Authors: B Movahedian, D Hasheminia
Format: Article
Language:fas
Published: Isfahan University of Medical Sciences 2008-01-01
Series:مجله دانشکده دندانپزشکی اصفهان
Subjects:
Online Access:http://jids.mui.ac.ir/index.php/jids/article/view/128