Congenital Adrenal Hyperplasia

Selma Feldman Witchel, Ricardo Azziz

Research output: Contribution to journalShort survey

52 Citations (Scopus)

Abstract

Congenital adrenal hyperplasia (CAH) due to P450c21 (21-hydroxylase deficiency) is a common autosomal recessive disorder. This disorder is due to mutations in the CYP21A2 gene which is located at chromosome 6p21. The clinical features reflect the magnitude of the loss of function mutations. Individuals with complete loss of function mutations usually present in the neonatal period. The clinical features of individuals with mild loss of function mutations are predominantly due to androgen excess rather than adrenal insufficiency leading to an ascertainment bias favoring diagnosis in females. Treatment goals include normal linear growth velocity and "on-time" puberty in affected children. For adolescent and adult women, treatment goals include regularization of menses, prevention of progression of hirsutism, and fertility. This article will review key aspects regarding pathophysiology, diagnosis, and treatment of CAH.

Original languageEnglish (US)
Pages (from-to)116-126
Number of pages11
JournalJournal of Pediatric and Adolescent Gynecology
Volume24
Issue number3
DOIs
StatePublished - Jun 1 2011

Fingerprint

Congenital Adrenal Hyperplasia
Mutation
Hirsutism
Adrenal Insufficiency
Menstruation
Puberty
Androgens
Fertility
Therapeutics
Chromosomes
Growth
Genes

Keywords

  • Ambiguous genitalia
  • Congenital adrenal hyperplasia
  • Hyperandrogenism
  • Premature adrenarche
  • Premature pubarche

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Obstetrics and Gynecology

Cite this

Congenital Adrenal Hyperplasia. / Witchel, Selma Feldman; Azziz, Ricardo.

In: Journal of Pediatric and Adolescent Gynecology, Vol. 24, No. 3, 01.06.2011, p. 116-126.

Research output: Contribution to journalShort survey

Witchel, Selma Feldman ; Azziz, Ricardo. / Congenital Adrenal Hyperplasia. In: Journal of Pediatric and Adolescent Gynecology. 2011 ; Vol. 24, No. 3. pp. 116-126.
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