MerlinDX Artikel E25.9
https://www.askep3s.org/aaf0c27ce3/artikel/E25.9
Artikel Klinis ICD-10: E25.9

E25.9: Gangguan Adrenogenital yang Tidak Specific (Adrenogenital Disorder, Unspecified)

1 menit baca Terverifikasi: 2026-08-05
Bagikan:

📚 Daftar Pustaka (APA 7)

[1]
Speiser PW, Arlt W, Auchus RJ, et al. Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline. J Clin Endocrinol Metab. 2018;103(11):4043-4088.
[2]
WHO. ICD-10 Version: 2016. Geneva: World Health Organization; 2016.
[3]
El-Maouche D, Arlt W, Merke DP. Congenital adrenal hyperplasia. Lancet. 2017;390(10108):2194-2210.
[4]
Nordenström A, Lajic S, Falhammar H. Long-term outcomes of congenital adrenal hyperplasia. Endocrinol Metab Clin North Am. 2021;50(2):199-215.
[5]
Turcu AF, Auchus RJ. Adrenal steroidogenesis and congenital adrenal hyperplasia. Endocrinol Metab Clin North Am. 2015;44(2):275-296.
[6]
Merke DP, Bornstein SR. Congenital adrenal hyperplasia. Lancet. 2005;365(9477):2125-2136.
[7]
Pallanza L, Guasti L, Gargantini E, et al. Molecular and clinical effects of mutations in congenital adrenal hyperplasia. Best Pract Res Clin Endocrinol Metab. 2021;35(2):101491.
[8]
Krone N, Haney A, White PC. Genetics and clinical characteristics of congenital adrenal hyperplasia. Rev Endocr Metab Disord. 2021;22(4):821-834.
[9]
Auchus RJ. The classic and nonclassic congenital adrenal hyperplasias. Endocrinol Metab Clin North Am. 2015;44(2):xi-xii.
[10]
Trapp CM, Oberfield SE. Recommendations for the diagnosis and management of congenital adrenal hyperplasia. Ann N Y Acad Sci. 2014;1317:1-7.

🔗 Konten Terkait: E25.9

Pathway: E25.9 Adrenogenital Disorder & SDKI