5,500.00 5,000.00

  • Description


The aim of newborn screening is to detect diagnostic markers of treatable disorders in blood spots collected from pre-symptomatic newborns. Early identification of disorders significantly improves the long-term prognosis of affected patients, minimizes complications, avoids unnecessary diagnostic testing and identifies families for whom prenatal genetic counseling may be helpful

  • Test Type:   Heel prick
  • Pre-test Information:  Clinical details and drug history must accompany sample.
  • Report Delivery:  Sample by Tue / Thu / Sat 5 pm; Report 2 days
  •   Components:  7