PL EN


2012 | 4 | 623-627
Article title

Wrodzony przerost nadnerczy – opis przypadku

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References
  • Speiser PW, Azziz R, Baskin LS, et al. Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society Clinical Practice Guideline. J Clin Endocrinol Metab 2010 September; 95(9): 4133–4160.
  • White PC. Congenital adrenal hyperplasia due to 17-hydroxylase deficiency. In: Kliegman RM, Stanton BF, St. Geme J,et al. eds. Nelson textbook of pediatrics. 19th ed. Philadelphia, Pa: Saunders Elsevier; 2011: chap 570.
  • Nimkarn S, Lin-Su K, New MI. Steroid 21 hydroxylase deficiency congenital adrenal hyperplasia. Pediatr Clin North Am 2011 Oct; 58(5):1281–300.
  • Henwood MJ, Levitt Katz LE. Disorders of the adrenal gland. In: T. Moshang, Jr. Pediatric endocrinology: the requisites in pediatrics. Philadelphia: Elsevier Mosby Inc. 2005: 63–72.
  • . Huynh T, McGown IT, Cowley D. The clinical and biochemical spectrum of congenital adrenal hyperplasia to 21-hydroxylase deficiency. Clin Biochem Rev 2009 May; 30(2): 75–86.
  • . Crown A, Lightman S. Why is the management of glucocorticoid deficiency still controversial: a review of the literature.Clin Endocrinol 2005; 63: 483–492.
  • Ghizzoni L, Cappa M, Chrousos G, et al. Pediatric adrenal diseases. Endocr Dev Basel, Karger 2011; 20: 129.
  • A. et al. Circadian hydrocortisone infusions in patients with adrenal insufficiency and congenital adrenal hyperplasia. Clin Endocrinol 2006; 65: 45–50
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