Article
Reproductive outcome of women with 21-hydroxylase-deficient nonclassic adrenal hyperplasia.
The Journal of clinical endocrinology and metabolism - 1 Sept 2006
Moran C, Azziz R, Weintrob N, Witchel S F, Rohmer V, Dewailly D, Marcondes J A M, Pugeat M, Speiser P W, Pignatelli D, Mendonca B B, Bachega T A S, Escobar-Morreale H F, Carmina E, Fruzzetti F, Kelestimur F
Abstract excerpt
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). OBJECTIVE: Our objective was to determine...
Topics
- Adrenal Hyperplasia, Congenital
- Adult
- Child, Preschool
- Female
- Genotype
- Humans
- Infant
- Infant, Newborn
- Male
- Pregnancy
- Prevalence
- Prospective Studies
- Retrospective Studies
- Steroid 21-Hydroxylase