Early diagnosis of 11 beta-hydroxylase deficiency in two siblings confirmed by analysis of a novel steroid metabolite in newborn urine

Acta Endocrinol (Copenh). 1986 Mar;111(3):349-54. doi: 10.1530/acta.0.1110349.

Abstract

Plasma and urinary steroid measurements are reported in 2 normotensive newborn female siblings with virilized external genitalia due to 11 beta-hydroxylase deficiency. Plasma 11-deoxycortisol concentrations were markedly elevated whereas 17OH-progesterone concentrations were not raised. Plasma renin activity was suppressed, but increased to levels characteristic of infancy within 4 weeks of treatment. The enzyme defect was confirmed by measurement of increased urinary excretion of tetrahydro-11-deoxycortisol. A more polar steroid metabolite, 6 alpha-hydroxytetrahydro-11-deoxycortisol was also determined by gas chromatographic and mass spectrometric analysis. Analysis of metabolites in urine is an additional specific marker to plasma 11-deoxycortisol measurement for the diagnosis of 11 beta-hydroxylase deficiency in early infancy.

MeSH terms

  • 17-Hydroxycorticosteroids / urine*
  • 17-alpha-Hydroxyprogesterone
  • Adrenal Hyperplasia, Congenital*
  • Androstenes / urine
  • Cortodoxone / analogs & derivatives
  • Cortodoxone / blood
  • Cortodoxone / urine*
  • Female
  • Humans
  • Hydrocortisone / blood
  • Hydroxyprogesterones / blood
  • Infant
  • Infant, Newborn
  • Renin / blood
  • Steroid Hydroxylases / deficiency*
  • Testosterone / blood
  • Virilism / diagnosis
  • Virilism / genetics*
  • Virilism / metabolism

Substances

  • 17-Hydroxycorticosteroids
  • Androstenes
  • Hydroxyprogesterones
  • Testosterone
  • tetrahydro-11-deoxycortisol
  • 17-alpha-Hydroxyprogesterone
  • Steroid Hydroxylases
  • Renin
  • Cortodoxone
  • Hydrocortisone