NEWBORN SCREENING PANEL 8
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.
Parameter(s) covered : 11
Report Frequency: Sample Mon / Wed / Fri by 9 am; Report Next day
Special Instruction: Clinical details and drug history is required.
Price : ₹ 2600.00
Parameters
- 17-OHP, NEONATAL
- Biotinidase Neonatal
- Cystic Fibrosis , Neonatal
- G6PD
- Galactosemia Neonatal
- Hb Pattern
- HbA
- HbA2
- HbF
- Phenylalanine Neonatal
- TSH, NEONATAL