Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline

Phyllis Speiser, Phyllis W Speiser, Wiebke Arlt, Auchus RJ, Richard J. Auchus, Laurence S. Baskin, Baskin LS, Conway GS, Gerard S Conway, Deborah P Merke, Merke DP, Heino F L Meyer-Bahlburg, Meyer-Bahlburg HFL, Walter L Miller, Miller WL, M Hassan Murad, Murad MH, Sharon E Oberfield, Oberfield SE, White PC, Perrin C White
The Journal of clinical endocrinology and metabolism · 2018 · vol. 103(11) , pp. 4043–4088 · doi:10.1210/jc.2018-01865 · PMID:30272171 · PMC6456929
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This Endocrine Society guideline updates clinical practice recommendations for managing congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency, incorporating evidence and expert opinion on patient safety, quality of life, cost, and utilization.

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Abstract

OBJECTIVE: To update the congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency clinical practice guideline published by the Endocrine Society in 2010. CONCLUSIONS: The writing committee presents updated best practice guidelines for the clinical management of congenital adrenal hyperplasia based on published evidence and expert opinion with added considerations for patient safety, quality of life, cost, and utilization.

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MeSH descriptors

Adrenal Hyperplasia, Congenital Endocrinology Societies, Medical Adrenal Hyperplasia, Congenital Adrenal Hyperplasia, Congenital Adrenal Hyperplasia, Congenital Adrenal Hyperplasia, Congenital Cost-Benefit Analysis Endocrinology Female Fetal Therapies Fetal Therapies Fetal Therapies Fetal Therapies Genetic Counseling Genetic Counseling Genetic Counseling Genetic Counseling Glucocorticoids Glucocorticoids

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