Following a low-phenylalanine diet can prevent intellectual disability and other complications in people with phenylketonuria. The diet focuses on low protein foods and avoids high protein foods.

Following a phenylketonuria diet is the main treatment for preventing serious symptoms. People with phenylketonuria (PKU) cannot break down the amino acid phenylalanine. Amino acids are organic ...

Only four days after Kala McWain’s son, Braxton, was born, she learned he had a rare condition called phenylketonuria (PKU). This means Braxton cannot eat protein and relies on a special diet ...

levels in adolescents with phenylketonuria (PKU) against only diet. The adolescent individuals in the trial are aged between 12 and 17 years. The open-label, randomised controlled trial is ...

A small percentage of people can't process phenylalanine because of a condition called phenylketonuria ... If you get too little tyrosine in your diet, your body will manufacture more.

PKU is a rare genetic disease that manifests ... At the moment the main treatment strategy is to restrict phe in the diet, a lifetime commitment that often requires nutritional supplements to ...

Pegvaliase statistically significantly lowered blood Phe levels in adolescents with PKU compared with diet alone. Topline data were announced from a phase 3 trial evaluating pegvaliase-pqpz in ...

It can be challenging for patients with PKU, or their caregivers, to keep on top of everything, like medication, medical formula, lab results and diet. The app is designed to offer flexible and ...