Dopa-responsive dystonia due to mild tyrosine hydroxylase deficiency

Ann Neurol. 2004 Jan;55(1):147-8. doi: 10.1002/ana.10820.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Amino Acid Metabolism, Inborn Errors / genetics
  • Brain Diseases, Metabolic / genetics
  • Dystonia / drug therapy*
  • Dystonia / etiology*
  • GTP Cyclohydrolase / genetics
  • Humans
  • Levodopa / therapeutic use*
  • Male
  • Mutation
  • Phenotype
  • Tyrosine 3-Monooxygenase / deficiency*
  • Tyrosine 3-Monooxygenase / genetics*

Substances

  • Levodopa
  • Tyrosine 3-Monooxygenase
  • GTP Cyclohydrolase