Diffusion-Weighted Imaging of White Matter Abnormalities in Patients with Phenylketonuria

Summary: Phenylketonuria (PKU) is an autosomal recessive disorder caused by a deficiency of the enzyme phenylalanine hydroxylase (EC 1.14.16.1). Affected patients develop elevated plasma and tissue levels of phenylalanine and its related ketoacids. Untreated patients usually exhibit severe mental re...

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Bibliografische gegevens
Gepubliceerd in:AJNR Am J Neuroradiol
Hoofdauteurs: Phillips, Micheal D., McGraw, Peter, Lowe, Mark J., Mathews, Vincent P., Hainline, Bryan E.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: American Society of Neuroradiology 2001
Onderwerpen:
Pediatrics
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7974588/
https://ncbi.nlm.nih.gov/pubmed/11559511
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