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HHH SYNDROME; HYPERORNITHINEMIA - HYPERAMMONEMIA - HOMOCITRULLINURIA SYNDROME

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.

  • Test Type:
  • Pre-test Information:
    Give brief clinical history
  • Report Delivery:
    Sample Daily by 5 pm; Report 5 days
  • Components:
    0

Sample Report