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 |
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Format: | Artikel |
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. |
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ISSN: | 1053-8119 1095-9572 |
DOI: | 10.1016/j.neuroimage.2006.04.154 |