MUCOPOLYSACCHARIDOSIS (MPS) SCREEN, URINE

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MUCOPOLYSACCHARIDOSIS (MPS) SCREEN, URINE

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Rs 462 Rs 350

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MUCOPOLYSACCHARIDOSIS (MPS) IS AN AUTOSOMAL RECESSIVE LYSOSOMAL STORAGE DISORDER. IT IS DUE TO THE DEFICIENCY OF THE ENZYME RESPONSIBLE FOR CATABOLISM OF GLYCOSAMINOGLYCANS (GAG). THESE PATIENTS FIRST PRESENT WITH INCREASED URINARY GAG EXCRETION.

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