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Comment
. 2019 Jun 1;104(6):1928.
doi: 10.1210/jc.2018-02629.

Response to Letter to the Editor: "Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline"

Phyllis W Speiser  1   2 , Richard J Auchus  3 , Deborah P Merke  4   5 , Walter L Miller  6 , Perrin C White  7
Affiliations
Comment

Response to Letter to the Editor: "Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline"

Phyllis W Speiser et al. J Clin Endocrinol Metab. .
No abstract available

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References

    1. Naiki Y, Fukami M. Letter to the Editor: “Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline.” J Clin Endocrinol Metab. 2019;104(6):1926–1927. - PubMed
    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. J Clin Endocrinol Metab. 2018;103(11):4043–4088. - PMC - PubMed
    1. Naiki Y, Miyado M, Horikawa R, Katsumata N, Onodera M, Pang S, Ogata T, Fukami M. Extra-adrenal induction of Cyp21a1 ameliorates systemic steroid metabolism in a mouse model of congenital adrenal hyperplasia. Endocr J. 2016;63(10):897–904. - PubMed
    1. Perdomini M, Dos Santos C, Goumeaux C, Blouin V, Bougnères P. An AAVrh10-CAG-CYP21-HA vector allows persistent correction of 21-hydroxylase deficiency in a Cyp21-/- mouse model. Gene Ther. 2017;24(5):275–281. - PubMed

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