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Genetic study in Egyptian children with wilson disease / Lamia Mohamed Hussein ; Supervised Ola Abdelmonem Elseesy , Hanaa Elkaraksy , Heba Sharaf Eldin

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Lamia Mohamed Hussein , 2013Description: 101 P. : charts , facsimiles ; 25cmOther title:
  • دراسة جينية لمرض ويلسون فى الاطفال المصريين [Added title page title]
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  • Issued also as CD
Dissertation note: Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Clinical and Chemical Pathology Summary: Background : Wilson disease (WD) is an autosomal recessive disorder caused by defects in the copper transporting P- type A TPase encoded by ATP7B gene resulting in deposition of copper mainly in liver and brain with significant disability or death if left untreated . An available regimen of treatment gives hope to those predisposed to the disease if diagnosed early
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Item type Current library Home library Call number Copy number Status Date due Barcode
Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.07.Ph.D.2013.La.G (Browse shelf(Opens below)) Not for loan 01010110062148000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.07.Ph.D.2013.La.G (Browse shelf(Opens below)) 62148.CD Not for loan 01020110062148000

Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Clinical and Chemical Pathology

Background : Wilson disease (WD) is an autosomal recessive disorder caused by defects in the copper transporting P- type A TPase encoded by ATP7B gene resulting in deposition of copper mainly in liver and brain with significant disability or death if left untreated . An available regimen of treatment gives hope to those predisposed to the disease if diagnosed early

Issued also as CD

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