When protein is eaten it is broken down by enzymes into amino acids (there are around 20 different amino acids). Amino acids are needed for a wide variety of functions within the body such as muscle maintenance, growth, repairing cells and tissues as well as making other body proteins and amino acids.
Phe is found in all foods containing protein. In PKU, the build-up of phe is due to the deficiency of an enzyme called phenylalanine hydroxylase. This PAH enzyme helps turn phe into another amino acid called tyrosine. This results in a build-up of phe and low levels of tyrosine. Both amino acids have important roles in the body. The build up of phe together with the reduction in tyrosine will lead to the person developing learning difficulties. The good news is if PKU is managed correctly from birth the development of learning difficulties can be completely avoided.
PKU can be different from person to person. Some people have no or very little PAH enzyme activity– this is referred to as classical or severe PKU. Some individuals have more PAH enzyme activity - this is called moderate or mild PKU. In the case of mild PKU, the term ‘Hyperphenylalanaemia’ (Hyperphe for short) is sometimes used.
For more information on the diet for PKU see Healthy Eating.
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