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Information Journal Paper

Title

MANAGEMENT OF THE THALASSEMIA-INDUCED SKELETAL FACIAL DEFORMITY: A CASE REPORT

Pages

  302-308

Abstract

THALASSEMIA syndrome is part of a larger group of inherited hematologic disorders known as hemoglobinopathies. SKELETAL changes resulting from this disease are striking and FACIAL bones are effected by this disease primarily. Orthodontic treatment are carried out to over come dentofacial deformities. However this method is not always successful and therefore orthognathic surgical management of the patient with THALASSEMIA could be required. A Case of THALASSEMIA major who had received this treatment is presented in this report.

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    APA: Copy

    MORTAZAVI, H., & SHAHROKHI, M.. (2001). MANAGEMENT OF THE THALASSEMIA-INDUCED SKELETAL FACIAL DEFORMITY: A CASE REPORT. JOURNAL OF DENTAL SCHOOL SHAHID BEHESHTI UNIVERSITY OF MEDICAL SCIENCE, 19(3), 302-308. SID. https://sid.ir/paper/22280/en

    Vancouver: Copy

    MORTAZAVI H., SHAHROKHI M.. MANAGEMENT OF THE THALASSEMIA-INDUCED SKELETAL FACIAL DEFORMITY: A CASE REPORT. JOURNAL OF DENTAL SCHOOL SHAHID BEHESHTI UNIVERSITY OF MEDICAL SCIENCE[Internet]. 2001;19(3):302-308. Available from: https://sid.ir/paper/22280/en

    IEEE: Copy

    H. MORTAZAVI, and M. SHAHROKHI, “MANAGEMENT OF THE THALASSEMIA-INDUCED SKELETAL FACIAL DEFORMITY: A CASE REPORT,” JOURNAL OF DENTAL SCHOOL SHAHID BEHESHTI UNIVERSITY OF MEDICAL SCIENCE, vol. 19, no. 3, pp. 302–308, 2001, [Online]. Available: https://sid.ir/paper/22280/en

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