PKU stands for Phenylketonuria. PKU is an inherited condition – a disorder of protein metabolism.
PKU is managed by a low protein diet, supplemented with protein substitutes to meet their nutritional needs. A child with PKU will be seen by a dietitian on a regular basis to help manage their condition.
Individuals with PKU must avoid high protein foods. These include:
Accidents can and will happen and there will be no immediate reaction if a child eats a food not permitted in their diet. This is different to the instant reaction that a child with a nut allergy may have. There is no need to seek medical attention.
No. Protein substitutes must not be mixed into foods or drinks.
The protein substitute needs to be treated like a medicine and taken in the full amount each day.