نوع مقاله : Original Article(s)
نویسندگان
1 استادیار و فوق تخصص غدد و متابولیسم کودکان، دانشکده پزشکی، دانشگاه علوم پزشکی قزوین، قزوین، ایران
2 دانشیار کودکان، دانشکده پزشکی، دانشگاه علوم پزشکی قزوین، قزوین، ایران
چکیده
عنوان مقاله [English]
نویسندگان [English]
Abstract Thalassemia is the most common hereditary anemia and beta thalassemia major is the most severe form of this syndrome. Patients' surveillance will be increase by the use of desferal, blood transfusion, and bone marrow transplantation, but simoultaneously the mineral bone density can be decreased. Background: In this cross- sectional study 63 patients with ß- thalassemia major (12-36 years old) were enrolled. Physical examination, laboratory tests, bone radiography and bone density measurements done for every one. Then, datas analyzed with SPSS software, and Chi- square test. Methods: 34 (56%) out of 63 patients were male. Patients mean age was 20/89 ± 5/01 years old, 11 ones (18%) were 12-17 and 52 patients (82%) were 17-36 years old. Mean of weight, height and BMI were 45/56 ± 9/2 Kg, 157 ± 10/43 cm and 19/87 ± 2/8 kg/m2 respectively. Impaired puberty observed in 27 ones (32/9%) and 40 (77%) had Low bone mineral density. The relationship between low bone mineral density and puberty status was significant (P < 0/05). Findings: This study shows a significant relation between low bone density (osteopenia, Osteoporosis) and impaired puberty in B. thalassemia major patients. Conclusion: Major thalassemia, Bone mineral density, Osteopenia, Osteoporosis, puberty. Key words:
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