Linking the degree of virilization in females with congenital adrenal hyperplasia to genotype. Issue 1 (22nd June 2017)
- Record Type:
- Journal Article
- Title:
- Linking the degree of virilization in females with congenital adrenal hyperplasia to genotype. Issue 1 (22nd June 2017)
- Main Title:
- Linking the degree of virilization in females with congenital adrenal hyperplasia to genotype
- Authors:
- Gurgov, Semyon
Bernabé, Kerlly J.
Stites, John
Cunniff, Christopher M.
Lin‐Su, Karen
Felsen, Diane
New, Maria I.
Poppas, Dix P. - Other Names:
- Zaidi Mone guestEditor.
- Abstract:
- Abstract: Mutations of CYP21A2 variably decrease 21‐hydroxylase activity and result in a spectrum of disease expressions in patients with congenital adrenal hyperplasia (CAH). We examined the association between CYP21A2 mutations and virilization (Prader score) in females with CAH. The study population included 187 CAH females with fully characterized CYP21A2 mutations. One hundred fifty‐eight patients were sorted into groups by expected enzyme activity (percent of normal activity) of the less severely affected allele: (A) null, 0%; (B) I2G, 1%; (C) I172N, 2%; and (D) V281L, >2%. We observed an inverse relationship between virilization and residual enzyme activity ( P < 0.001). Subjects in group A or B had a significantly higher likelihood (unadjusted odds ratio: 16; P < 0.001) of developing severe virilization compared with those in group C. Surprisingly, 24% of group D patients, whose mutation is usually associated with nonclassical (NC) CAH, had severe virilization. Among subjects with the NC P30L mutation, 66% expressed unexpected virilization. Virilization, usually leading to extensive reconstructive surgery, is highly likely in patients with null or I2G mutations; however, NC mutations (P30L/V281L) may also lead to unexpected virilization. These findings have implications for prenatal counseling and highlight the need for additional investigations into other factors that influence virilization in CAH.
- Is Part Of:
- Annals of the New York Academy of Sciences. Volume 1402:Issue 1(2017)
- Journal:
- Annals of the New York Academy of Sciences
- Issue:
- Volume 1402:Issue 1(2017)
- Issue Display:
- Volume 1402, Issue 1 (2017)
- Year:
- 2017
- Volume:
- 1402
- Issue:
- 1
- Issue Sort Value:
- 2017-1402-0001-0000
- Page Start:
- 56
- Page End:
- 63
- Publication Date:
- 2017-06-22
- Subjects:
- congenital adrenal hyperplasia -- P30L mutation -- genital atypia -- genetic mutation -- virilization
Medical sciences -- Periodicals
Medicine -- Periodicals
Science -- Periodicals
610 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1749-6632 ↗
http://www.blackwellpublishing.com/journal.asp?ref=0077-8923&site=1 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/nyas.13370 ↗
- Languages:
- English
- ISSNs:
- 0077-8923
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 1031.000000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4752.xml