Phenylketonuria (PKU) is a genetic condition that occurs in 1 out of 15,000 people - males and females. It interferes with the breakdown of phenylalanine, a normal part of protein. Too much phenylalanine can affect brain development and lead to mental retardation. Individuals with PKU can be treated with a low-phenylalanine diet and lead completely normal, healthy lives.
In Wisconsin, all newborns have been screened for PKU since 1965. The state of Wisconsin provides special low phenylalanine formula and some low-protein foods and baking products to individuals with PKU to help these children develop normally.
Clinic staff follows more than 100 children and adults with PKU. An experienced team of specialists provides diagnosis and management of PKU. The PKU team includes certified gentic counselors and metabolic dietitians.
In addition, referrals are made to Neuropsychology on an as-needed basis for developmental evaluations and family functioning assessments.
Locations
The PKU clinic is located on Level I of the Curative Care Network building, across the parking lot from Children's Hospital. Enter the north door (which faces the Children's Hospital parking structure) and take the elevator to Level I. Free parking is available in the Children's Hospital visitor lot or parking structure. Parking for a fee is available at Curative.
Information on PKU can be confusing and recommendations have changed over the years. If you have any questions about the status of you or your child, or if you would like to speak with someone about PKU, please call (414) 266-3347.
