Identification of some different types of mucopolysaecharidoses disease in affected children in Egyptian population by biophysical and biochemical methods / Azza Mahamoud Abdellatef Deghaidy ; Supervised Azza Orabi , Waffaa Ahmed Khalil , Salwa Mohamed Youssef
Material type:
- التعرف على بعض الانواع المختلفة لأمراض السكريات المتعددة المخاطبة فى الأطفال المصابين فى التجمعات السكانية المصرية بواسطة الطرق الفيزيائية الحيوية و الكيميائية الحيوية [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 | Cai01.12.04.Ph.D.2009.Az.I (Browse shelf(Opens below)) | Not for loan | 01010110052339000 | ||
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مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.12.04.Ph.D.2009.Az.I (Browse shelf(Opens below)) | 52339.CD | Not for loan | 01020110052339000 |
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Thesis (Ph.D.) - Cairo University - Faculty of Science - Department of Biophysics
MPS are inheritable disorders caused by deficiency of lysosomal enzymes. The most commonly detected clinical manifestation were coarse facies and mental retardation in all cases followed by hepatosplenomegaly, skeletal deformity, cataracts umblical hemia, heart affection and hearing affection. Our study detected increase in the activity of hyaluronidase in leukocytes in MPS patients
Issued also as CD
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