PHENYLALANINE, NEWBORN SCREEN
Phenylketonuria (PKU) is the most common autosomal recessive inherited disorder of amino acid metabolism caused by deficiency of enzyme Phenylalanine hydroxylase. This assay is useful for evaluating patients with Hyperphenylalaninemia and monitoring effectiveness of dietary therapy.
Parameter(s) covered : 1
Report Frequency: Sample Mon through Fri by 9 am; Report Next day
Special Instruction: Clinical details and drug history must accompany sample.
Price : ₹ 280.00
Parameters
- PHENYLALANINE, NEWBORN SCREEN