Reproductive outcome of women with 21-hydroxylase-deficient nonclassic adrenal hyperplasia
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, vol.91, no.9, pp.3451-3456, 2006 (SCI-Expanded, Scopus)
- Publication Type: Article / Article
- Volume: 91 Issue: 9
- Publication Date: 2006
- Doi Number: 10.1210/jc.2006-0062
- Journal Name: JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
- Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Page Numbers: pp.3451-3456
- Erciyes University Affiliated: Yes
Abstract
Context: Because many women with 21-hydroxylase (21-OH)-deficient nonclassic adrenal hyperplasia (NCAH) carry at least one allele affected by a severe mutation of CYP21, they are at risk for giving birth to infants with classic adrenal hyperplasia (CAH).