Congenital adrenal hyperplasia in adults

Karen Lin-Su, Saroj Nimkarn, Maria I. New

Research output: Contribution to journalReview articlepeer-review

2 Scopus citations

Abstract

Hyperandrogenism in congenital adrenal hyperplasia (CAH) results from overstimulation of adrenocorticotropic-driven androgen production in the adrenal cortex due to lack of cortisol feedback. The classical form is characterized by more-severe symptoms of hyperandrogenism, including virilization of the female genitalia. The milder nonclassical form presents with postnatal symptoms of hyperandrogenism. Presenting symptoms in adulthood may include acne, male-pattern alopecia, hirsutism, irregular menses/amenorrhea or infertility. The goal of therapy in CAH is to both correct the deficiency in cortisol secretion and suppress androgen overproduction. Glucocorticoid replacement has been the mainstay of treatment for CAH but new treatment strategies continue to be developed and studied.

Original languageEnglish
Pages (from-to)67-77
Number of pages11
JournalExpert Review of Endocrinology and Metabolism
Volume4
Issue number1
DOIs
StatePublished - 2009

Keywords

  • 21-hydroxylase
  • Androgen excess
  • Bone mineral density
  • Congenital adrenal hyperplasia
  • Cytochrome P450 21A2
  • Fertility
  • Glucocorticoid replacement
  • Hirsutism
  • Polycystic ovarian syndrome

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