Reproductive outcome of women with 21-hydroxylase-deficient nonclassic adrenal hyperplasia

Moran, Hasan; Azziz, R.; Weintrob, N.; Witchel, S.; Rohmer, V.; Dewailly, D.; Marcondes, J.; Pugeat, M.; Speiser, P.; Pignatelli, D.; Mendonca, B.; Bachega, T.; Escobar-Morreale, H.; Carmina, E.; Fruzzetti, F.; Kelestimur, F.

doi:10.1210/jc.2006-0062

Reproductive outcome of women with 21-hydroxylase-deficient nonclassic adrenal hyperplasia

Moran C., Azziz R., Weintrob N., Witchel S. F., Rohmer V., Dewailly D., ...Daha Fazla

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, cilt.91, sa.9, ss.3451-3456, 2006 (SCI-Expanded, Scopus)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 91 Sayı: 9
Basım Tarihi: 2006
Doi Numarası: 10.1210/jc.2006-0062
Dergi Adı: JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
Sayfa Sayıları: ss.3451-3456
Erciyes Üniversitesi Adresli: Evet

Özet

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).