PHENYLALANINE

Phenylketonuria is one of the most common autosomal recessively inherited disorders. It affects the metabolism of amino acids by deficiency of the enzyme, Phenylalanine hydroxylase. The test is used to evaluate patients who suffer from Hyperphenylalaninemia and is also used to monitor the effectiveness of the diet-based therapy.


How to prepare for the test?

Clinical details and drug history must accompany the sample.

Book Your Test

*All fields are mandatory.
Home sample collection charges will be applicable.