Special Instruction : Clinical details and drug history is required.
Parameters covered : 7
Report Frequency : Sample Mon through Fri by 9 am; Report Next day
Home Collection
Lab Visit
Newborn babies should be screened for congenital disorders which if missed at birth can lead to serious side effects such as lifelong damage of nervous system, intellectual, physical & developmental disabilities. Early detection of these defects improves long term clinical condition, minimizes complications & avoids unnecessary diagnostic tests. It also identifies families who require genetic counselling. This test panel checks for thyroid disease, deficiency of important enzymes namely G6PD & Biotinidase and for evidence of other diseases like Galactosemia, Phenylketonuria (PKU), Cystic fibrosis & Congenital adrenal hyperplasia (CAH) .
1. 17-OHP, NEONATAL
2. Biotinidase Neonatal
3. Cystic Fibrosis , Neonatal
4. G6PD
5. Galactosemia Neonatal
6. Phenylalanine Neonatal
7. TSH, NEONATAL
Clinical details and drug history is required.
Sample Mon through Fri by 9 am; Report Next day
Z335
Congenital Metabolic Disorders
2 hrs
1 week
1 week
Fluoroimmunoassay
1 drop of heel prick Blood each on 3 spots of filter paper available from LPL. Ship refrigerated or frozen. Clinical details and drug history must accompany sample.
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.
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