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Health Information and Tools >  Phenylketonuria (PKU) Test

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Phenylketonuria (PKU) Test

Test Overview

A phenylketonuria (PKU) test is done to check whether a newborn baby has the enzyme needed to use phenylalanine in their 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 have a screening test for PKU to find out if the baby has an increased risk of the disease. 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. The test may be repeated within the first week or two after birth.

Information about Phenylketonuria (PKU) Test

Adaptation Date: 02/25/2022

Adapted By: Alberta Health Services

Adaptation Reviewed By: Alberta Health Services

Adapted with permission from copyrighted materials from Ignite Healthwise, LLC (Healthwise). This information does not replace the advice of a doctor. Healthwise disclaims any warranty and is not responsible or liable for your use of this information. Your use of this information means that you agree to the Terms of Use. How this information was developed to help you make better health decisions.

Information about Phenylketonuria (PKU) Test

Adaptation Date: 02/25/2022

Adapted By: Alberta Health Services

Adaptation Reviewed By: Alberta Health Services