High-dose fludrocortisone therapy was transiently required in a female neonate with 21-hydroxylase deficiency-Reference-Cited by-同舟云学术

High-dose fludrocortisone therapy was transiently required in a female neonate with 21-hydroxylase deficiency

Published:2022 Issue:2 Volume:31 Page:93-97
ISSN:0918-5739
Container-title:Clinical Pediatric Endocrinology
language:en
Short-container-title:Clin Pediatr Endocrinol

Author:

Kawasaki Yusuke¹,Sato Takeshi¹,Nakano Satsuki¹,Usui Takeshi²,Narumi Satoshi³,Ishii Tomohiro¹,Hasegawa Tomonobu⁴

Affiliation:

1. Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan

2. Research Support Center, Shizuoka General Hospital, Shizuoka, Japan

3. Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan

4. The Center for Differences of Sex Development, Keio University Hospital, Tokyo, Japan

Publisher

Japanese Society for Pediatric Endocrinology

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health

Link

https://www.jstage.jst.go.jp/article/cpe/31/2/31_2021-0066/_pdf

Reference11 articles.

1. 1. Turcu, AF, Auchus, RJ. Adrenal steroidogenesis and congenital adrenal hyperplasia. Endocrinol Metab Clin North Am 2015;44: 275–96.

2. 2. Riepe, FG, Sippell, WG. Recent advances in diagnosis, treatment, and outcome of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Rev Endocr Metab Disord 2007;8: 349–63.

3. 3. White, PC. Congenital Adrenal Hyperplasia Caused by 21-Hydroxylase Deficiency. In: Kliegman RM, St Geme III JW, Blum NJ, Shah SS, Tasker RC, Wilson KM, editors. Nelson Textbook of Pediatrics, 21st edition. Philadelphia: Elsevier; 2019.p.2971–6.

4. 4. Koyama, Y, Homma, K, Fukami, M, Miwa, M, Ikeda, K, Ogata, T, et al. Classic and non-classic 21-hydroxylase deficiency can be discriminated from P450 oxidoreductase deficiency in Japanese infants by urinary steroid metabolites. Clin Pediatr Endocrinol 2016;25: 37–44.

5. 5. Nimkarn, S, Gangishetti, PK, Yau, M, New, MI. 21-hydroxylase-deficient congenital adrenal hyperplasia. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mirzaa G, Amemiya A, editors. 21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia. University of Washington, Seattle; 2016:1993-2021.GeneReviews® [Internet].

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