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) identifier identifier identifier

  • 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).