A phenylketonuria (PKU) test is done to check whether a newborn baby has the enzyme needed to use phenylalanine in his or her body. Phenylalanine is an amino acid that is needed for normal growth and development. If a baby's body does not have the enzyme that changes phenylalanine into another amino acid called tyrosine, the phenylalanine level builds up in the baby's blood and can cause brain damage, seizures, and intellectual disability.
The damage caused by PKU can begin weeks after the baby has started drinking breast milk or formula. Babies with PKU need foods low in phenylalanine to prevent severe brain damage. Phenylalanine is found in most foods that have protein, such as milk, cheese, and meats.
It is important to find this disease early. All babies in Canada and the United States are tested for PKU right after birth. To have the disease, you must inherit the gene from each parent.
The blood sample for PKU is usually taken from your baby's heel (called a heel stick). The test is done in the first few days after birth, as early as 24 hours after birth. In some areas, the test may be repeated within the first week or two after birth.
A phenylketonuria (PKU) screening test is done to see whether a newborn baby has the enzyme needed to use phenylalanine in his or her body. If this test shows that your baby has a phenylalanine problem, the doctor will do further testing to check whether your baby has PKU.
It's important for your baby to have this screening test soon after birth. If a baby has PKU and treatment starts right away, problems (such as brain damage) are less likely to occur.
You do not need to do anything before your baby has this test.
Your baby's heel is cleaned with alcohol, and then the heel is poked with a small needle. Several drops of blood are collected inside circles on a special piece of paper. When enough blood has been collected, a small bandage is put on the site.
Your baby may feel a sting or a pinch with a heel stick.
Usually, there are no problems from a heel stick. A small bruise may develop.
A phenylketonuria (PKU) test is done to check whether a new baby has the enzyme needed to use phenylalanine in his or her body.
Less than 265 micromoles per litre (mcmol/L) or 3 milligrams per decilitre (mg/dL)
If the heel stick screening test shows high phenylalanine levels, a blood sample is taken from your baby's vein to confirm whether he or she has PKU.
Reasons the results may not be helpful include:
Chernecky CC, Berger BJ (2013). Laboratory Tests and Diagnostic Procedures, 6th ed. St. Louis: Saunders.
Other Works Consulted
Committee on Genetics, American Academy of Pediatrics (2008). Maternal phenylketonuria. Pediatrics, 122(2): 445-449.
Fischbach FT, Dunning MB III, eds. (2009). Manual of Laboratory and Diagnostic Tests, 8th ed. Philadelphia: Lippincott Williams and Wilkins.
March of Dimes (2013). Birth defects: PKU in your baby. Available online: http://www.marchofdimes.com/baby/birthdefects_pku.html.
Pagana KD, Pagana TJ (2010). Mosby's Manual of Diagnostic and Laboratory Tests, 4th ed. St. Louis: Mosby Elsevier.
ByHealthwise StaffPrimary Medical ReviewerJohn Pope, MD - PediatricsThomas M. Bailey, MD - Family MedicineKathleen Romito, MD - Family MedicineSpecialist Medical ReviewerChuck Norlin, MD - Pediatrics
Current as ofMay 4, 2017
Current as of: May 4, 2017
John Pope, MD - Pediatrics
& Thomas M. Bailey, MD - Family Medicine & Kathleen Romito, MD - Family Medicine & Chuck Norlin, MD - Pediatrics
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