PKU dietary handbook to accompany PKU guidelines

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 co...

Full description

Bibliographic Details
Main Authors: A. MacDonald, A. M. J. van Wegberg, K. Ahring, S. Beblo, A. Bélanger-Quintana, A. Burlina, J. Campistol, T. Coşkun, F. Feillet, M. Giżewska, S. C. Huijbregts, V. Leuzzi, F. Maillot, A. C. Muntau, J. C. Rocha, C. Romani, F. Trefz, F. J. van Spronsen
Format: Article
Language:English
Published: BMC 2020-06-01
Series:Orphanet Journal of Rare Diseases
Subjects:
Phenylketonuria
PKU
Diet
Treatment
Recommendations
Guidelines
Online Access:http://link.springer.com/article/10.1186/s13023-020-01391-y

Internet

http://link.springer.com/article/10.1186/s13023-020-01391-y

Similar Items