Study of some biochemical markers in female patients with transfusion dependent Ý-thalassemia / Noha Sayed Hamed Awad ; Supervised Mervat Elsayed Mohamed , Mohamed Ali Eldesouky , Samir Mostafa Abdelaziz
Material type:
- دراسه بعض الدلالات الكيميائيه الحيويه فى الأناث المصابات بأنيميا البحر المتوسط و المعتمدات على نقل الدم [Added title page title]
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قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.12.02.Ph.D.2017.No.S (Browse shelf(Opens below)) | Not for loan | 01010110073933000 | ||
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مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.12.02.Ph.D.2017.No.S (Browse shelf(Opens below)) | 73933.CD | Not for loan | 01020110073933000 |
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Thesis (Ph.D.) - Cairo University - Faculty of Science - Department of Biochemistry
The deleterious effect of iron overload on anti-müllerian hormone (AMH) level, as a best test to investigate ovarian reserve, was evaluated in 90 female patients with thalassemia major (TM), intermedia (TI) and minor, osteoporosis detection through measurement of bone mineral density (BMD z-score) using DXA and laboratory diagnosis. Also, to investigate the effects of iron chelation therapy including deferiprone and deferoxamine in the management of transfusion-related iron overload. The present results revealed that Serum AMH level was lower in female patients with transfusion dependent Ý-thalassemia than in thalassemia minor also, Ferritin was 25 fold more in thalassemia major compared to thalassemia minor (3088.0±2497.6 ng/ml vs. 120.3±36.2 ng/ml). There was significant negative correlation of AMH with ferritin in all thalassemic females. The prevalence rate of osteoporosis, based on the WHO criteria was 3.3% in thalassemia major and the prevalence of osteopenia was 93.3% in thalassemia major and 30% in thalassemia intermedia. The present finding implied a significantly higher ferritin, higher PTH, higher osteocalcin and lower AMH in patients with thalassemia major that used deferoxamine than deferiprone. In conclusion, patients with thalassemia major and intermedia constitute a high risk group due to higher ferritin concentrations and iron overload
Issued also as CD
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