Prenatal Diagnosis and Treatment in Congenital Adrenal Hyperplasia
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Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-030-82591-1_9
Reference67 articles.
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2. White PC. Update on diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Curr Opin Endocrinol Diabetes Obes. 2018;25:178–84. https://doi.org/10.1097/MED.0000000000000402.
3. Harada F, Kimura A, Iwanaga T, Shomizawa K, Yata J, Sasazuki T. Gene conversion-like events cause steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia. Proc Natl Acad Sci U S A. 1987;84:8091–4. https://doi.org/10.1073/pnas.84.22.8091.
4. Speiser PW, Arlt W, Auchus RJ, Baskin LS, Conway GS, Merke DP, et al. Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an endocrine society clinical practice guideline. J Clin Endocrinol Metab. 2018;103:4043–88. https://doi.org/10.1210/jc.2018-01865.
5. New MI, Abraham M, Yuen T, Lekarev O. An update on prenatal diagnosis and treatment of congenital adrenal hyperplasia. Semin Reprod Med. 2012;30:396–9. https://doi.org/10.1055/s-0032-1324723.
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