Nutritional management of phenylalanine hydroxylase (PAH) deficiency in pediatric patients in Canada: a survey of dietitians’ current practices

BACKGROUND: Phenylalanine hydroxylase (PAH) deficiency is one of 31 targeted inherited metabolic diseases (IMD) for the Canadian Inherited Metabolic Diseases Research Network (CIMDRN). Early diagnosis and initiation of treatment through newborn screening has gradually shifted treatment goals from th...

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Detalles Bibliográficos
Autores principales: Yuskiv, Nataliya, Potter, Beth K., Stockler, Sylvia, Ueda, Keiko, Giezen, Alette, Cheng, Barbara, Langley, Erica, Ratko, Suzanne, Austin, Valerie, Chapman, Maggie, Chakraborty, Pranesh, Collet, Jean Paul, Pender, Amy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6323774/
https://www.ncbi.nlm.nih.gov/pubmed/30621767
http://dx.doi.org/10.1186/s13023-018-0978-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6323774/
https://www.ncbi.nlm.nih.gov/pubmed/30621767
http://dx.doi.org/10.1186/s13023-018-0978-0

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