IDENTIFICATION OF SOME DIFFERENT TYPES OF MUCOPOLYSAECHARIDOSES DISEASE IN AFFECTED CHILDREN IN EGYPTIAN POPULATION BY BIOPHYSICAL AND BIOCHEMICAL METHODS
Azza Mahamoud Abd-El-Latef Deghaidy;
Abstract
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 her
The most commonly detected clinical manifestation were coarse facies and mental
retardation in all cases followed by hepatosplenomegaly, skeletal deformity, cataracts
umblical her
Other data
| Title | IDENTIFICATION OF SOME DIFFERENT TYPES OF MUCOPOLYSAECHARIDOSES DISEASE IN AFFECTED CHILDREN IN EGYPTIAN POPULATION BY BIOPHYSICAL AND BIOCHEMICAL METHODS | Other Titles | التعرف على بعض الأنواع المختلفة لأمراض السكريات المتعددة المخاطية في الأطفال المصابين في التجمعات السكانية المصرية بواسطة الطرق الفيزيائية والكيماوية الحيوية | Authors | Azza Mahamoud Abd-El-Latef Deghaidy | Keywords | IDENTIFICATION OF SOME DIFFERENT TYPES OF MUCOPOLYSAECHARIDOSES DISEASE IN AFFECTED CHILDREN IN EGYPTIAN POPULATION BY BIOPHYSICAL AND BIOCHEMICAL METHODS | Issue Date | 2009 | Description | 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 her |
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| File | Size | Format | |
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| 94500r2319.pdf | 311.97 kB | Adobe PDF | View/Open |
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