Atypical phenylketonuria caused by 7, 8-dihydrobiopterin synthetase deficiency

Lancet. 1979 Jan 20;1(8108):131-3. doi: 10.1016/s0140-6736(79)90521-x.

Abstract

A patient with atypical phenylketonuria and normal liver dihydropteridine reductase and phenylalanine-4-hydroxylase activities excreted neopterin but not biopterin or dihydrobiopterin in urine. The oral administration of L-sepiapterin (1 mg/kg body weight) lowered serum-henylalanine from 17.1 to 1.1 mg/dl within 6 h. Comparable responses were observed after oral administration of L-erythro-7, 8-dihydrobiopterin or L-erythro-5, 6, 7, 8-tetrahydrobiopterin (each given in a dose of 2.5 mg/kg body weight). The results indicate a 7, 8-dihydrobiopterin synthetase deficiency in the patient.

Publication types

  • Case Reports

MeSH terms

  • Alcohol Oxidoreductases / deficiency*
  • Biopterins / analogs & derivatives
  • Biopterins / biosynthesis*
  • Biopterins / deficiency
  • Biopterins / urine
  • Child, Preschool
  • Female
  • Guanosine Triphosphate / metabolism
  • Humans
  • Phenylalanine / antagonists & inhibitors
  • Phenylalanine / blood
  • Phenylketonurias / drug therapy
  • Phenylketonurias / etiology*
  • Phenylketonurias / metabolism
  • Pteridines / biosynthesis*
  • Pteridines / therapeutic use
  • Pterins

Substances

  • Pteridines
  • Pterins
  • Biopterins
  • Phenylalanine
  • 7,8-dihydrobiopterin
  • Guanosine Triphosphate
  • sepiapterin
  • Alcohol Oxidoreductases