[21 hydroxylase deficiency: new strategies emerging from molecular studies]

Ann Endocrinol (Paris). 2003 Dec;64(6):456-70.
[Article in French]
No abstract available

MeSH terms

  • Adrenal Hyperplasia, Congenital / diagnosis*
  • Adrenal Hyperplasia, Congenital / enzymology
  • Adrenal Hyperplasia, Congenital / genetics
  • Amino Acid Substitution
  • Case Management
  • Chromosomes, Human, Pair 6 / genetics
  • Dexamethasone / therapeutic use
  • Female
  • Fetal Diseases / diagnosis
  • Fetal Diseases / drug therapy
  • Fetal Diseases / enzymology
  • Fetal Diseases / genetics
  • Genes, Recessive
  • Genetic Carrier Screening
  • Genetic Counseling
  • Humans
  • Point Mutation
  • Pregnancy
  • Prenatal Diagnosis
  • Steroid 21-Hydroxylase / genetics*
  • Virilism / etiology
  • Virilism / prevention & control

Substances

  • Dexamethasone
  • Steroid 21-Hydroxylase