Non-classic congenital adrenal hyperplasia.

  title={Non-classic congenital adrenal hyperplasia.},
  author={Selma Feldman Witchel},
  volume={78 8},
Non-classic or late-onset congenital adrenal hyperplasia (NCAH) due to 21-hydroxylase deficiency is one of the most common autosomal recessive disorders. Reported prevalence is approximately 1 in 1000. Affected individuals typically present due to signs and symptoms of androgen excess. The purpose of this review is to provide current information regarding the pathophysiology, molecular genetics, and management of this common disorder. The treatment of NCAH needs to be directed towards the… CONTINUE READING


Publications citing this paper.
Showing 1-8 of 8 extracted citations

Non-Classical Congenital Adrenal Hyperplasia in Childhood

Journal of clinical research in pediatric endocrinology • 2017

May AMH levels distinguish LOCAH from PCOS among hirsute women?

European journal of obstetrics, gynecology, and reproductive biology • 2014
View 2 Excerpts

Similar Papers

Loading similar papers…