HHH SYNDROME; HYPERORNITHINEMIA - HYPERAMMONEMIA - HOMOCITRULLINURIA SYNDROME

  • Test Usage:
    HHH syndrome is a defect of Urea cycle metabolism inherited as an autosomal recessive disorder. It may be present at birth, during childhood or even adulthood. It is characterized by lethargy, poor feeding, vomiting, encephalopathy and liver dysfunction.
  • Report Availability:
    Sample Daily by 5 pm; Report 5 days
  • Sample Report:
5 Diagnostic Centers found for HHH SYNDROME; HYPERORNITHINEMIA - HYPERAMMONEMIA - HOMOCITRULLINURIA SYNDROME 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