TY  - BOOK
AU  - Azza Mahamoud Abdellatef Deghaidy
AU  - Azza Orabi , 
AU  - Salwa Mohamed Youssef , 
AU  - Waffaa Ahmed Khalil , 
TI  - Identification of some different types of mucopolysaecharidoses disease in affected children in Egyptian population by biophysical and biochemical methods / 
PY  - 2009///
CY  - Cairo : 
PB  - Azza Mahamoud Abdellatef Deghaidy , 
KW  - Human-hyaluronidases sulfite oxidase
KW  - Lysosomal enzymes
KW  - MPS
N1  - Thesis (Ph.D.) - Cairo University - Faculty of Science - Department of Biophysics; Issued also as CD
N2  - 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
UR  - http://172.23.153.220/th.pdf
ER  -