Journal of Biochemistry and Biotechnology

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Journal of Biochemistry and Biotechnology 44 7897 074717

Mucopolysaccharidoses Neonatal Disease Impact Factor

Mucopolysaccharidoses (MPS) are lysosomal storage diseases during which mutations of genes encoding for lysosomal enzymes cause defects within the degradation of glycosaminoglycans (GAGs). the buildup of GAGs in lysosomes leads to cellular dysfunction and clinical abnormalities. Mucopolysaccharidoses (MPS) are lysosomal storage diseases during which mutations of genes encoding for lysosomal enzymes cause defects within the degradation of glycosaminoglycans (GAGs). the buildup of GAGs in lysosomes leads to cellular dysfunction and clinical abnormalities. the first initiation of enzyme replacement therapy (ERT) can slow or prevent the event of severe clinical manifestations. Infants who failed the recheck at recall were mentioned MacKay Memorial Hospital for detailed confirmatory diagnosis.

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