Osteoporosis in Transfusion Dependent Thalassemia

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HASHEMIEH MOZHGAN

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Journal Paper

Paper Information

Journal: Journal of Arak University Medical Sciences Year:2019 | Volume:22 | Issue:5 Page(s): 2-5

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Information Journal Paper

Title

Osteoporosis in Transfusion Dependent Thalassemia

Author(s)

HASHEMIEH MOZHGAN | Issue Writer Certificate

Keywords

Not Registered.

Abstract

-thalassemia syndromes are the most prevalent quantitative hereditary hemoglobinopathies in the world. One of the most debilitating complications in thalassemia patients is osteoporosis and osteopenia which predisposes them to skeletal pain and pathologic fractures. Osteoporosis was more prevalent in patients with thalassemia intermedia compared to thalassemia major. . . .

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References

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APA: Copy

HASHEMIEH, MOZHGAN. (2019). Osteoporosis in Transfusion Dependent Thalassemia. ARAK MEDICAL UNIVERSITY JOURNAL (AMUJ), 22(5 ), 2-5. SID. https://sid.ir/paper/69176/en

Vancouver: Copy

HASHEMIEH MOZHGAN. Osteoporosis in Transfusion Dependent Thalassemia. ARAK MEDICAL UNIVERSITY JOURNAL (AMUJ)[Internet]. 2019;22(5 ):2-5. Available from: https://sid.ir/paper/69176/en

IEEE: Copy

MOZHGAN HASHEMIEH, “Osteoporosis in Transfusion Dependent Thalassemia,” ARAK MEDICAL UNIVERSITY JOURNAL (AMUJ), vol. 22, no. 5 , pp. 2–5, 2019, [Online]. Available: https://sid.ir/paper/69176/en

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