Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia

Ann N Y Acad Sci. 1985:458:111-29. doi: 10.1111/j.1749-6632.1985.tb14597.x.
No abstract available

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 17-alpha-Hydroxyprogesterone
  • Adrenal Hyperplasia, Congenital* / diagnosis*
  • Amniotic Fluid / analysis
  • Diagnostic Errors
  • Ethics, Medical
  • Female
  • Fetal Diseases / diagnosis*
  • Follow-Up Studies
  • Genotype
  • Histocompatibility Testing
  • Humans
  • Hydroxyprogesterones / analysis
  • Infant, Newborn
  • Male
  • Pedigree
  • Pregnancy
  • Prenatal Diagnosis*
  • Risk
  • Sodium / metabolism
  • Steroid Hydroxylases / deficiency*

Substances

  • Hydroxyprogesterones
  • 17-alpha-Hydroxyprogesterone
  • Sodium
  • Steroid Hydroxylases