MUCOPOLYSACCHARIDOSIS (MPS) SCREEN, URINE
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.
Parameter(s) covered : 1
Report Frequency: Sample Daily by 4 pm; Report Next day
Special Instruction: First morning urine sample required. Provide brief clinical and drug history.
Price : ₹ 390.00
Parameters
- MUCOPOLYSACCHARIDOSIS (MPS) SCREEN, URINE