PKU is a genetic disorder. It requires lifetime dietary and medical management. There is currently no cure for PKU; research continues, and many advances have been made.
Once diagnosed (usually within 3-5 days of birth), your newborn is referred to a PKU specialist. In Minnesota, patients with PKU may be referred to the University of Minnesota PKU Clinic, Children’s Hospital, or the Mayo Clinic.
Your newborn is placed on a protein restricted diet and carefully monitored. Their diet includes a protein supplement that can come in many different forms. A liquid formula is the most commonly used treatment.
