Genetic study in Egyptian children with wilson disease / Lamia Mohamed Hussein ; Supervised Ola Abdelmonem Elseesy , Hanaa Elkaraksy , Heba Sharaf Eldin
Material type: TextLanguage: 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]
- Issued also as CD
Item type | Current library | Home library | Call number | Copy number | Status | Date due | Barcode | |
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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 | 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 |
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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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