Mucopolysacchari dosis (MPS) is an autosomal recessive lysosomal storage disorder. It is due to the deficiency of the enzyme responsible for catabolism of glycosaminoglycan s (GAG). These patients first present with increased urinary GAG excretion.
Sample Type - Urine
Reporting Time - 1 Day
Prerequisites - No special preparation required
Price - ₹430/-
Add to cart Go Home