Role of parathormone and altered calcium homeostasis in bone disease in Egyptian adult patients with thalassemia / Salwa Hassan Ahmed Ali ; Supervised Alia Abdelaziz Saad , Hala Mahmoud Fahmy , Mohamed Talaat
Material type:
TextLanguage: English Publication details: Cairo : Salwa Hassan Ahmed Ali , 2014Description: 162 P. : charts , facsimiles ; 25cmOther title: - دراسة دور هرمون الغدة الجاردرقية و خلل نسبة الكالسيوم بالجسم على العظام فى مرضى الثلاسيما المصريين البالغين [Added title page title]
- Issued also as CD
| Item type | Current library | Home library | Call number | Copy number | Status | Barcode | |
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Thesis
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قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.18.M.Sc.2014.Sa.R (Browse shelf(Opens below)) | Not for loan | 01010110064329000 | ||
CD - Rom
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مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.18.M.Sc.2014.Sa.R (Browse shelf(Opens below)) | 64329.CD | Not for loan | 01020110064329000 |
Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Internal Medicine
Beta Thalassemia is the most common chronic hemolytic anemia in Egypt (85.1%). Iron overload remains the biggest threat to the health of patients with thalassemia. Multi - transfused thalassaemic patients may develop severe endocrine complications due to iron overload. Etiology of bone disease in thalassemic patients is poorly understood. Number of studies has examined the effect of various conditions on the pathogenesis of bone disease including ineffective erythropoiesis, iron overload, vitamin D concentrations, and the influence of endocrinopathies. Hypopara-thyroidism was found in 7.6% of a group of thalassemic patients in Iran but 3.6 {u2013} 7% reported in Italian thalassemic patients
Issued also as CD
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