PKU is an inherited disorder that causes the amino acid phenylalanine to build up in the body. ... “PKU is like when you can’t have certain foods that other people can have,” said Conner.

A Brampton dad is set to take on a 372-mile run from Bristol to Newcastle to raise funds for a rare disease charity.

Since newborns with phenylketonuria (PKU) do not initially have any symptoms, the first step in treating PKU is timely ...

Phenylketonuria (PKU) is a rare newborn genetic disease that impacts between 1 in 10,000 to 1 in 20,000 people, depending on the individuals' genetic ancestry. PKU causes an amino acid - called ...

A small study of people with a rare disorder ... that its engineered version of the bacteria provided some benefit to patients with a rare genetic disease called phenylketonuria, or PKU. People ...

Hudson said his sister, Tia, lives with Phenylketonuria (PKU) which is an inherited metabolic disease affecting the brain. People living with PKU cannot process a substance called phenylalanine ...

The European Commission has approved PTC Therapeutics' treatment for the rare disease phenylketonuria (PKU), Sephience, ...

People gathered outside the Enniskillen Castle which was illuminated in green on Saturday June 28 to show support for the PKU ...

PTC Therapeutics’ Sephience gets European marketing authorization to treat children and adults living with phenylketonuria: Warren, New Jersey Tuesday, June 24, 2025, 14:00 Hrs ...