header
Local cover image
Local cover image
Image from OpenLibrary

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

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Azza Mahamoud Abdellatef Deghaidy , 2009Description: 176 Leaves : charts ; 30cmOther title:
  • 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]
Subject(s): Online resources: Available additional physical forms:
  • Issued also as CD
Dissertation note: Thesis (Ph.D.) - Cairo University - Faculty of Science - Department of Biophysics Summary: 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
Tags from this library: No tags from this library for this title. Log in to add tags.
Star ratings
    Average rating: 0.0 (0 votes)
Holdings
Item type Current library Home library Call number Copy number Status Barcode
Thesis Thesis 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
CD - Rom CD - Rom 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

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

There are no comments on this title.

to post a comment.

Click on an image to view it in the image viewer

Local cover image