OBJECTIVE: To review all available data and recommend a definition for polycystic ovary
syndrome (PCOS) based on published peer-reviewed data, whether already in use or not, to …

Non-classic congenital adrenal hyperplasia (NCAH) is a relatively common disorder
regardless of ethnicity, but most cases are never diagnosed, especially in males. A baseline …

Objective To update the congenital adrenal hyperplasia due to steroid 21-hydroxylase
deficiency clinical practice guideline published by the Endocrine Society in 2010 …

Objective: We developed clinical practice guidelines for congenital adrenal hyperplasia
(CAH). Participants: The Task Force included a chair, selected by The Endocrine Society …

Congenital adrenal hyperplasias (CAH) are inherited defects of cortisol biosynthesis. More
than 90% of CAH are caused by 21-hydroxylase deficiency (21-OHD), found in 1: 10 000 to …

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 …

Nonclassic congenital adrenal hyperplasia (NCAH) is one of the most frequent autosomal
recessive disorders in man with a prevalence ranging from 0.1% in Caucasians up to a few …

Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is one of the most
common autosomal recessive disorders. The aim of this study was to assess the frequencies …

Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is caused by
mutations in the CYP21A2 gene and is often fatal in its classic forms if not treated with …

Background Nonclassical congenital adrenal hyperplasia (NC‐CAH) is caused by mutations
of the CYP21A2 gene. The clinical manifestations and hormonal derangements of NC‐CAH …