Metachromatic leukodystrophy in Egyptian children with dysmyelinating brain disease / Lamiaa Tarek Mohamed Tawfik ; Supervised Fayza Abdelhamid Hassan , Laila Abdelmoteleb Selim , Nahla Aly Fawzy Fayek
Material type: TextLanguage: English Publication details: Cairo : Lamiaa Tarek Mohamed Tawfik , 2011Description: 107 P. : charts ; 25cmOther title:- ضمور المادة البيضاء (الميتاكروماتيك) بين امراض اعتلال المادة البيضاء في الأطفال 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.M.Sc.2011.La.M (Browse shelf(Opens below)) | Not for loan | 01010110057580000 | |||
CD - Rom | مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.11.07.M.Sc.2011.La.M (Browse shelf(Opens below)) | 57580.CD | Not for loan | 01020110057580000 |
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Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Clinical and Chemical Pathology
Metachromatic leukodystrophy (MLD) is an autosomal recessive neurodegenerative disease caused by a deficiency of the lysosomal enzyme aryl sulfatase A (ARSA). To detect MLD cases among twenty patients presenting with symptoms of cerebral white matter disease and evidence of while matter affection by MRI. ARSA enzyme activity was estimated in blood leucocytes for all patients
Issued also as CD
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