NBS Phenylketonuria (Phenylalanine)
Overview of NBS Phenylketonuria (Phenylalanine) in Thane
The NBS Phenylketonuria (Phenylalanine) test is a newborn screening test used to detect Phenylketonuria (PKU), a rare inherited metabolic disorder in which the body is unable to properly break down an amino acid called phenylalanine. When phenylalanine accumulates in the blood, it can become toxic and may affect brain development and nervous system function. Early identification through newborn screening allows timely dietary management, helping prevent serious complications and ensuring healthy growth and development.
Who Should Get This Test Done?
This test is recommended for:
● All newborn babies as part of routine newborn screening programs
● Infants with a family history of Phenylketonuria (PKU)
● Newborns born to parents known to be carriers of PKU-related genetic mutations
● Babies showing signs of metabolic disorders, although symptoms may not be present in the newborn period
● Infants requiring follow-up testing after an abnormal newborn screening result
Why Consider This Test?
Phenylketonuria can cause irreversible intellectual disability, developmental delays, behavioural problems, and neurological complications if left untreated. Since symptoms often do not appear immediately after birth, newborn screening plays a critical role in early detection. Identifying elevated phenylalanine levels soon after birth enables prompt dietary intervention, which can significantly reduce the risk of long-term complications and support normal physical and cognitive development.
More Information About the Test
This test is typically performed using a few drops of blood collected from the baby’s heel, usually within the first few days after birth. The sample is analysed to measure phenylalanine levels in the blood. Elevated levels may indicate PKU or another disorder affecting phenylalanine metabolism and may require confirmatory testing. The test is a part of newborn screening (NBS) programs designed to detect serious but treatable conditions before symptoms develop.
Other Names
● Newborn Screening for Phenylketonuria
● PKU Screening Test
● Phenylalanine Screening Test
● Newborn Phenylalanine Test
● Phenylketonuria (PKU) Newborn Screen
● NBS PKU Test
Test included
- Phenylalanine
Doctor information
Test code
3312
CPT and Loinc codes
Department
- Eia-neonatal
Turn around time
Next Day
Test run frequency
Monday,Thursday TIME - 10:30
Performing locations
4 labs across India
Specimen vol. and vacutainer information
| Specimen | Vacutainer | Volume |
|---|---|---|
| Blood Spot | NeoNatal Cards | 1 |
Specimen stability information
Blood Spot
Collection instructions
Complete CLINICAL HISTORY form including birth date & birth time.(Dried Blood spot should be ideally collected within 2nd and 5th day of life after birth).Avoid touching and smearing of the blood spots.The dried blood specimen should be transported or mailed to the laboratory as soon as they are dry (Minimum of 3 Hrs.) and no later than 24 hrs after collection.
Package price
₹485
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₹485