MUCOPOLYSACCHARIDOSIS (MPS) SCREEN, URINE

MUCOPOLYSACCHARIDOSIS (MPS) SCREEN, URINE

257 Ratings

Rs 466 Rs 350

25 % OFF

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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10 ML (5 ML MIN.) ALIQUOT OF FIRST MORNING URINE IN A STERILE SCREW CAPPED CONTAINER. DO NOT USE ANY PRESERVATIVES. SHIP REFRIGERATED OR FROZEN. PROVIDE BRIEF CLINICAL AND DRUG HISTORY.

TOLUIDINE BLUE SPOT TEST

REPORT ON 4TH DAY EVENING 7PM

FIRST MORNING URINE SAMPLE REQUIRED. PROVIDE BRIEF CLINICAL AND DRUG HISTORY.

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