Reduced cerebral DOPA uptake in adult patients suffering from phenylketonuria

Aim: In phenylketonuria (PKU), the lack of phenylalanin-hydroxylase causes an excess of phenylalanine in all body compartments. Since phenylalanine and tyrosine compete for the same transport system in neurons, synthesizing dopamine from tyrosine in PKU patients with elevated phenylalanine values, a...

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Veröffentlicht in:NeuroImage (Orlando, Fla.) Fla.), 2006, Vol.31, p.T171-T171
Hauptverfasser: Landvogt, Christian, Mengel, E., Buchholz, H.-G., Siessmeier, T., Zepp, F., Ullrich, K., Bartenstein, P.
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Sprache:eng
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Zusammenfassung:Aim: In phenylketonuria (PKU), the lack of phenylalanin-hydroxylase causes an excess of phenylalanine in all body compartments. Since phenylalanine and tyrosine compete for the same transport system in neurons, synthesizing dopamine from tyrosine in PKU patients with elevated phenylalanine values, a decrease of dopamine levels can be expected.
ISSN:1053-8119
1095-9572
DOI:10.1016/j.neuroimage.2006.04.154