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Gonadal function in adult Egyptian thalassemic patients / Sara Elsayed Abdelghani Anter ; Supervised Mona Mansour Abdelrahman , Nehad Mohamed Tawfeek , Nahed Mohamed Ibrahim

By: Contributor(s): Material type: TextLanguage: English Publication details: Cairo : Sara Elsayed Abdelghani Anter , 2014Description: 228 P. : charts ; 25cmOther title:
  • وظائف الغدد التناسلية فى مرضى أنيميا البحر المتوسط البالغين فى مصر [Added title page title]
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Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Internal Medicine Summary: Thalassemia is an inherited autosomal recessive blood disorder. Early and regular blood transfusion therapy in patients with homozygous Ý- thalassemia decreases the complications of sever anemia and prolongs suvival but the beneficial effects of trausfusion are limited by organ damage from iron overload. Well chelated patients are fertile. Non chelated patients suffer from hypogonadism
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Item type Current library Home library Call number Copy number Status Barcode
Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.18.M.Sc.2014.Sa.G (Browse shelf(Opens below)) Not for loan 01010110064392000
CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.18.M.Sc.2014.Sa.G (Browse shelf(Opens below)) 64392.CD Not for loan 01020110064392000

Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Internal Medicine

Thalassemia is an inherited autosomal recessive blood disorder. Early and regular blood transfusion therapy in patients with homozygous Ý- thalassemia decreases the complications of sever anemia and prolongs suvival but the beneficial effects of trausfusion are limited by organ damage from iron overload. Well chelated patients are fertile. Non chelated patients suffer from hypogonadism

Issued also as CD

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