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Phenylketonuria (PKU) is a rare genetic condition in which the body cannot break down an amino acid called phenylalanine (say "fehn-uhl-AL-uh-neen"), which is a part of protein. This substance is found in breast milk, many types of baby formula, and most foods, especially those with a lot of protein, such as meat, eggs, and dairy products. If PKU is not treated, phenylalanine can build up in the blood and lead to intellectual disability and problems with the central nervous system (brain and spinal cord).
Early treatment can help prevent most problems. Babies born with PKU need to start treatment soon after birth.
Phenylketonuria (PKU) is passed down through families. To have the disease, a baby must get (inherit) the PKU gene from both parents. The father and mother may not have PKU or even know that PKU runs in their families. A baby who gets the gene from only one parent is a carrier of the PKU gene but does not have the disease.
If you have a child with PKU and are thinking about having another baby, you may want to get genetic counselling. If you have a family history of PKU, talk with your doctor about genetic testing if you want to find out whether you carry the gene.
If phenylketonuria (PKU) is not found and treated soon after birth, symptoms usually start to appear within a few months after birth. (It takes time for the phenylalanine to build up in the baby's body.)
Early symptoms of PKU in a baby may include:
Without early treatment, the child may have growth problems, developmental delays, seizures, and severe intellectual disability.
Screening is recommended for all newborns within a few days after birth. footnote 1
If the phenylketonuria (PKU) screening test shows that your baby has a phenylalanine problem, the doctor will do further testing to check whether your baby has PKU.
Finding and starting treatment for PKU early usually can prevent brain damage and other long-term problems.
The main treatment for phenylketonuria (PKU) is a lifelong reduced-protein diet. Problems are less likely to occur if your baby starts a PKU diet by age 3 weeks. Your baby's doctor can help you choose a formula that doesn't contain phenylalanine. You may be able to feed your baby some breast milk, but talk to your baby's doctor first. As your child gets older, a registered dietitian can help you choose the right foods and recipes.
The medicine sapropterin (Kuvan) may help lower phenylalanine levels in some children who have PKU. More studies are needed to find out the health effects from long-term use. With or without the medicine, your child still needs to follow a PKU diet.
Your child will need regular blood tests. Your child may get tested as often as once or more a week for the first year and then once or twice a month throughout childhood.
It's normal to feel a wide range of emotions when your child has an illness like PKU. You may want to join a support group. Your doctor can also help.
People who have phenylketonuria (PKU) need to follow a reduced-protein diet throughout their lives. For a few people, treatment with sapropterin (Kuvan) may help when used with a PKU diet. Talk to your doctor about the pros and cons of this medicine.
You'll need regular blood tests to check your phenylalanine level. If the level builds up, it can affect your IQ and your ability to learn, think, and understand.
Any woman with PKU who is planning to have a baby needs to be very careful to control her phenylalanine levels. Babies born to mothers who have high levels of phenylalanine are at risk for having a very small head, intellectual disability, growth problems, and heart problems. Having regular blood tests and following the PKU diet before and during pregnancy can help protect the baby.
CitationsCommunity Paediatrics Committee, Fetus and Newborn Committee (2019). Your newborn: Bringing baby home. Caring for Kids. https://www.caringforkids.cps.ca/handouts/pregnancy-and-babies/bringing_baby_home. Accessed April 30, 2021.
Current as of: August 2, 2022
Author: Healthwise StaffMedical Review: John Pope MD - PediatricsKathleen Romito MD - Family Medicine
Current as of: August 2, 2022
Author: Healthwise Staff
Medical Review:John Pope MD - Pediatrics & Kathleen Romito MD - Family Medicine
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