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, ss.3451-3456, 2006 (SCI İndekslerine Giren Dergi) identifier identifier identifier

  • Cilt numarası: 91 Konu: 9
  • Basım Tarihi: 2006
  • Doi Numarası: 10.1210/jc.2006-0062
  • Dergi Adı: JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
  • Sayfa Sayıları: ss.3451-3456

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).