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PKU dietary handbook to accompany PKU guidelines.


ABSTRACT: BACKGROUND:Phenylketonuria (PKU) is an autosomal recessive inborn error of phenylalanine metabolism caused by deficiency in the enzyme phenylalanine hydroxylase that converts phenylalanine into tyrosine. MAIN BODY:In 2017 the first European PKU Guidelines were published. These guidelines contained evidence based and/or expert opinion recommendations regarding diagnosis, treatment and care for patients with PKU of all ages. This manuscript is a supplement containing the practical application of the dietary treatment. CONCLUSION:This handbook can support dietitians, nutritionists and physicians in starting, adjusting and maintaining dietary treatment.

SUBMITTER: MacDonald A 

PROVIDER: S-EPMC7329487 | BioStudies | 2020-01-01

REPOSITORIES: biostudies

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