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. 1983 Jun;58(6):457–458. doi: 10.1136/adc.58.6.457

Management of the extrapyramidal manifestations of phenylketonuria with L-dopa

M D MacLeod, J F Munro, J G Ledingham, J W Farquhar
PMCID: PMC1627972  PMID: 6859941

Abstract

We report on a patient with phenylketonuria who developed disabling extrapyramidal features that were successfully controlled with L-dopa. We recommend that all such patients are given a trial with this drug.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Curtius H. C., Baerlocher K., Völlmin J. A. Pathogenesis of phenylketonuria: inhibition of DOPA and catecholamine synthesis in patients with phenylketonuria. Clin Chim Acta. 1972 Nov;42(1):235–239. doi: 10.1016/0009-8981(72)90406-8. [DOI] [PubMed] [Google Scholar]
  2. FARQUHAR J. W., RICHMOND J., TAIT H. P. PHENYLKETONURIA IN PEDIATRIC PRACTICE. Clin Pediatr (Phila) 1963 Sep;2:504–516. doi: 10.1177/000992286300200908. [DOI] [PubMed] [Google Scholar]
  3. PAINE R. S. The variability in manifestations of untreated patients with phenylketonuria (phenylpyruvic aciduria). Pediatrics. 1957 Aug;20(2):290–302. [PubMed] [Google Scholar]

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