Psychiatric and Cognitive Aspects of Phenylketonuria: The Limitations of Diet and Promise of New Treatments

Phenylketonuria (PKU) is a recessive disorder of phenylalanine metabolism due to mutations in the gene for phenylalanine hydroxylase (PAH). Reduced PAH activity results in significant hyperphenylalaninemia, which leads to alterations in cerebral myelin and protein synthesis, as well as reduced level...

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Detalles Bibliográficos
Autores principales: Ashe, Killian, Kelso, Wendy, Farrand, Sarah, Panetta, Julie, Fazio, Tim, De Jong, Gerard, Walterfang, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Psychiatry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6748028/
https://www.ncbi.nlm.nih.gov/pubmed/31551819
http://dx.doi.org/10.3389/fpsyt.2019.00561

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6748028/
https://www.ncbi.nlm.nih.gov/pubmed/31551819
http://dx.doi.org/10.3389/fpsyt.2019.00561

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