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

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Amerah Mohamed Ahmed Elshahawy

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TextLanguage: English Publication details: Cairo : Amerah Mohamed Ahmed Elshahawy , 2012Description: 123 P. : facsimiles ; 25cmOther title:

أنيميا إنحلال الدم الحادة كعرض أولى لمرض ويلسون [Added title page title]

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Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Pediatrics Summary: 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

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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	Cai01.11.28.M.Sc.2012.Am.A (Browse shelf(Opens below))		Not for loan	01010110058167000
CD - Rom	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

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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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