Nonclassical congenital adrenal hyperplasia: targets of treatment and transition.

@article{McCannCrosby2014NonclassicalCA,
  title={Nonclassical congenital adrenal hyperplasia: targets of treatment and transition.},
  author={Bonnie M McCann-Crosby and M. Chen and Sarah K Lyons and Yuezhen Lin and Marni E Axelrad and Jennifer E. Dietrich and Vernon Reid Sutton and Charles Gilbert Macias and Sheila K Gunn and Lefkothea P Karaviti},
  journal={Pediatric endocrinology reviews : PER},
  year={2014},
  volume={12 2},
  pages={224-38}
}
Nonclassical congenital adrenal hyperplasia (NCCAH) caused by 21-hydroxylase deficiency is a common autosomal recessive condition that can present with a wide range of hyperandrogenemic signs in childhood or adulthood. The management of children with NCCAH can be challenging, as no universally accepted guidelines have been established. Our goal was to evaluate the literature and develop an evidence-based guideline for the medical management of children and adolescents with NCCAH. We reviewed… CONTINUE READING
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