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 long term prognosis of affected patients, minimizes complications, avoids unnecessary diagnostic testing and identifies families for whom pre-natal genetic counselling 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:

Sample Report