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:
71 Diagnostic Centers found for HHH SYNDROME; HYPERORNITHINEMIA - HYPERAMMONEMIA - HOMOCITRULLINURIA SYNDROME in Ghaziabad