Citrullinaemia: an infantile form with p-hydroxyphenylpyruvic and p-hydroxyphenyllactic acidurias

J Inherit Metab Dis. 1987;10(3):276. doi: 10.1007/BF01800080.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Amino Acid Metabolism, Inborn Errors / drug therapy
  • Amino Acid Metabolism, Inborn Errors / metabolism*
  • Benzoates / therapeutic use
  • Benzoic Acid
  • Citrulline / blood*
  • Female
  • Humans
  • Infant
  • Phenylpropionates / urine*
  • Phenylpyruvic Acids / urine*
  • Tyrosine / metabolism*

Substances

  • Benzoates
  • Phenylpropionates
  • Phenylpyruvic Acids
  • 4-hydroxyphenylpyruvic acid
  • Citrulline
  • 4-hydroxyphenyllactic acid
  • Tyrosine
  • Benzoic Acid