Screening for late onset congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Indian J Med Res. 1990 Apr:92:79-82.

Abstract

Basal and post-ACTH levels of 17 alpha hydroxy-progesterone (17 OHP) were determined in 53 subjects with hirsutism. Late onset congenital adrenal hyperplasia (LOCAH) was detected in five (10.6%) on the basis of elevated basal and/or ACTH stimulated levels of 17 OHP. Of the five patients, two were considered to have a heterogygous state on account of a small rise in stimulated 17 alpha OHP. Screening tests for LOCAH are essential as the clinical diagnosis is not otherwise possible for this treatable and often familial disorder.

MeSH terms

  • 17-alpha-Hydroxyprogesterone
  • Adrenal Glands / pathology*
  • Adrenal Hyperplasia, Congenital*
  • Adrenocorticotropic Hormone / pharmacology
  • Adult
  • Female
  • Hirsutism / blood
  • Hirsutism / complications
  • Humans
  • Hydroxyprogesterones / blood
  • Hyperplasia
  • Prospective Studies
  • Steroid Hydroxylases / deficiency*

Substances

  • Hydroxyprogesterones
  • 17-alpha-Hydroxyprogesterone
  • Adrenocorticotropic Hormone
  • Steroid Hydroxylases