Clinical_Rounds_in_Endocrinology_Volume_II_-_Pediatric_Endocrinology

(singke) #1

376



  1. Kaye CI, Committee on Genetics, Accurso F, et al. Newborn screening fact sheets. Pediatrics.
    2006;118:e934.

  2. Krone N, Arlt W. Genetics of congenital adrenal hyperplasia. Baillieres Best Pract Res Clin
    Endocrinol Metab. 2009;23:181–92.

  3. Melmed S, Williams R. Williams textbook of endocrinology. Philadelphia: Elsevier/Saunders;
    2011.

  4. Mercè Fernández-Balsells M, Muthusamy K, Smushkin G, et al. Prenatal dexamethasone use
    for the prevention of virilization in pregnancies at risk for classical congenital adrenal hyper-
    plasia because of 21-hydroxylase (CYP21A2) defi ciency: a systematic review and meta-
    analyses. Clin Endocrinol (Oxf). 2010;73:436–44.

  5. Merke DP, Bornstein SR. Congenital adrenal hyperplasia. Lancet. 2005;365:2125–36.

  6. Merke DP, Keil MF, Jones JV, Fields J, Hill S, Cutler Jr GB. Flutamide, testolactone, and
    reduced hydrocortisone dose maintain normal growth velocity and bone maturation despite
    elevated androgen levels in children with congenital adrenal hyperplasia. J Clin Endocrinol
    Metab. 2000;85:1114–20.

  7. Nimkarn S, Lin-Su K, New M. Steroid 21-hydroxylase defi ciency congenital adrenal hyper-
    plasia. Pediatr Clin North Am. 2011;58:1281–300.

  8. Speiser P, Azziz R, Baskin L, Ghizzoni L, Hensle T, Merke D, et al. Congenital adrenal hyper-
    plasia due to steroid 21-hydroxylase defi ciency: an Endocrine Society Clinical Practice
    Guideline. J Clin Endocrinol Metab. 2010;95:4133–60.


10 Congenital Adrenal Hyperplasia
Free download pdf