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Review

Congenital Adrenal Hyperplasia: Diagnosis and Emergency Treatment

In: Endotext [Internet]. South Dartmouth (MA): MDText.com, Inc.; 2000.
.
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Review

Congenital Adrenal Hyperplasia: Diagnosis and Emergency Treatment

Mabel Yau et al.
Free Books & Documents
No abstract available

Copyright © 2000-2026, MDText.com, Inc.

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GUIDELINES

    1. Speiser PW, Arlt W, Auchus RJ, Baskin LS, Conway GS, Merke DP, Meyer-Bahlburg HFL, Miller WL, Murad MH, Oberfield SE, White PC. Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline. - PMC - PubMed
    1. J Clin Endocrinol Metab. 2018 Nov 1;103(11):4043–4088. - PMC - PubMed
    1. Rodriguez A, Ezquieta B, Labarta JI, Clemente M, Espino R, Rodriguez A, et al. Recommendations for the diagnosis and treatment of classic forms of 21-hydroxylase-deficient congenital adrenal hyperplasia. An Pediatr (Barc). 2017;87(2):116 e1- e10. - PubMed

References

    1. New M, Yau M, Lekarev O, Lin-Su K, Parsa A, Pina C, Yuen T, Khattab A. Congenital Adrenal Hyperplasia. In: Feingold KR, Anawalt B, Boyce A, Chrousos G, Dungan K, Grossman A, Hershman JM, Kaltsas G, Koch C, Kopp P, Korbonits M, McLachlan R, Morley JE, New M, Perreault L, Purnell J, Rebar R, Singer F, Trence DL, Vinik A, Wilson DP, editors. Endotext [Internet]. South Dartmouth (MA):MDText.com, Inc.; 2000-2017 Mar 15
    1. El-Maouche D, Arlt W, Merke DP. Congenital adrenal hyperplasia. Lancet. 2017 Nov 11;390(10108):2194–2210. - PubMed
    1. Fluck CE, Miller WL. P450 oxidoreductase deficiency: a new form of congenital adrenal hyperplasia. Curr Opin Pediatr. 2006;18(4):435–41. - PubMed
    1. Yilmaz R, Sahin D, Aghayev A, Erol OB, Poyrazoglu S, Saka N, et al. Sonography and Magnetic Resonance Imaging Characteristics of Testicular Adrenal Rest Tumors. Pol J Radiol. 2017;82:583–8. - PMC - PubMed
    1. New MI, Abraham M, Gonzalez B, Dumic M, Razzaghy-Azar M, Chitayat D, et al. Genotype-phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency. Proc Natl Acad Sci U S A. 2013;110(7):2611–6. - PMC - PubMed

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