Acute hemolytic anemia as an initial presentation of wilson's disease / Amerah Mohamed Ahmed Elshahawy ; Supervised Mona Elsaid Elraziky , Mona Mohamed Hamdy , Amal Abdelhamid Ali
Material type:
- أنيميا إنحلال الدم الحادة كعرض أولى لمرض ويلسون [Added title page title]
- Issued also as CD
Item type | Current library | Home library | Call number | Copy number | Status | Barcode | |
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قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.28.M.Sc.2012.Am.A (Browse shelf(Opens below)) | Not for loan | 01010110058167000 | ||
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مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.28.M.Sc.2012.Am.A (Browse shelf(Opens below)) | 58167.CD | Not for loan | 01020110058167000 |
Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Pediatrics
Wilson's disease (WD) is an autosomal recessive inherited disorder of copper metabolism resulting in pathological accumulation of copper in many organs and tissues. Hemolytic anemia (HA) in WD occurs in up to 17% of patients at some point in time during the natural course of illness. The aim of current study was to screen for WD among children presenting HA
Issued also as CD
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