Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency

Clin Endocrinol (Oxf). 1998 Oct;49(4):411-7. doi: 10.1046/j.1365-2265.1998.00559.x.
No abstract available

Publication types

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

MeSH terms

  • Adrenal Cortex Hormones / therapeutic use
  • Adrenal Hyperplasia, Congenital / diagnosis
  • Adrenal Hyperplasia, Congenital / drug therapy
  • Adrenal Hyperplasia, Congenital / etiology*
  • Female
  • Gene Deletion
  • Genotype
  • Hormones / therapeutic use
  • Humans
  • Infant, Newborn
  • Male
  • Mutation
  • Phenotype
  • Pregnancy
  • Prenatal Diagnosis
  • Steroid 21-Hydroxylase / genetics*

Substances

  • Adrenal Cortex Hormones
  • Hormones
  • Steroid 21-Hydroxylase