Pseudogene/functional gene ratio in late-onset 21-hydroxylase-deficient adrenal hyperplasia
- Ricardo Azziz(corresponding author),
- Gretchen Wells,
- Ronald T. Acton,
- Howard A. Zacur
- University of Alabama at Birmingham,
- Johns Hopkins University
Abstract
Late-onset adrenal hyperplasia caused by 21-hydroxylase deficiency leads to hyperandrogenic symptoms in 1% to 6% of hyperandrogenic women. Normally there are two 21-hydroxylase genes present in a 1 : 1 ratio. Gene CYP21A is a nonfunctional pseudogene, whereas CYP21B is an active gene. Abnormalities of the CYP21A CYP21B gene ratio may serve as a marker for late-onset adrenal hyperplasia. Eight hyperandrogenic patients with late-onset adrenal hyperplasia and five control subjects were studied by evaluation of autoradiograms of Taq I and Kpn I digests by means of laser densitometry. Seven of eight (87%) patients with late-onset adrenal hyperplasia had an abnormal CYP21A CYP21B gene ratio on laser densitometry, suggestive of CYP21A gene duplication, CYP21B gene deletion, or the conversion of a CYP21B gene to a CYP21A gene. One of the five control subjects had a heterozygous deletion of the CYP21A gene. The CYP21A CYP21B gene ratio may serve as a useful genetic marker for late-onset adrenal hyperplasia in a non-high-risk population.
Publication Information
Output type
Original language
English (US)Pages from-to (Number of pages)
Pages 633-638 (6 pages)Journal (Volume, Issue Number)
American journal of obstetrics and gynecology (Volume 162, Issue 3)Publication milestones
- Published - 03/1990
Publication status
ISSN
0002-9378Publication IDs
- Scopus: 0025253309
- PubMed: 2316563
