MUCOPOLYSACCHARIDOSIS (MPS) SCREEN, URINE

  • Test Usage:
    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.
  • Report Availability:
    Sample Daily by 4 pm; Report Next day
  • Sample Report:
5 Diagnostic Centers found for MUCOPOLYSACCHARIDOSIS (MPS) SCREEN, URINE in Chandigarh
  • DR. LAL PATH LABS , BOOTH NO- 3, SEC 19D, CHANDIAGRH , PIN CODE - 160019


    0172 5019886

    psc.chandigarh2@lalpathlabs.com

    Collection Center
  • Booth No. 343, Sector 32 D, Chandigarh-160032


    9953972272, 9953959260

    psc.chandigarh@lalpathlabs.com

    Collection Center
  • DR.LAL PATH LABS , BOOTH NO- 336, SECTOR- 44D, CHANDIGARH-160047


    0172 5019885

    psc.chandigarh3@lalpathlabs.com

    Collection Center
  • Booth No.-31, Sector 47C, Chandigarh-160047


    0172 5034135

    psc.chandigarh47@lalpathlabs.com

    Collection Center
  • Booth No-100, Sector-38C, Chandigarh-160036


    0172-5019887

    Psc.chandigarh4@lalpathlabs.com

    Collection Center