Clinical guidelines for the diagnosis and treatment of 21-hydroxylase deficiency (2021 revision)-Reference-Cited by-同舟云学术

Clinical guidelines for the diagnosis and treatment of 21-hydroxylase deficiency (2021 revision)

Published:2022 Issue:3 Volume:31 Page:116-143
ISSN:0918-5739
Container-title:Clinical Pediatric Endocrinology
language:en
Short-container-title:Clin Pediatr Endocrinol

Author:

Ishii Tomohiro¹,Kashimada Kenichi¹,Amano Naoko²,Takasawa Kei³,Nakamura-Utsunomiya Akari⁴,Yatsuga Shuichi⁵,Mukai Tokuo⁶,Ida Shinobu¹,Isobe Mitsuhisa⁷,Fukushi Masaru⁷,Satoh Hiroyuki⁸,Yoshino Kaoru⁹,Otsuki Michio¹⁰,Katabami Takuyuki¹⁰,Tajima Toshihiro⁴

Affiliation:

1. Differences of Sex Development (DSD) and Adrenal Disorders Committee, Japanese Society for Pediatric Endocrinology

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

3. Department of Pediatrics and Developmental Biology, Tokyo Medical and Dental University (TMDU), Tokyo, Japan

4. Committee on Mass Screening, Japanese Society for Pediatric Endocrinology

5. Department of Pediatrics, Fukuoka University School of Medicine, Fukuoka, Japan

6. Department of Pediatrics, Asahikawa Red Cross Hospital, Asahikawa, Japan

7. Japanese Society for Neonatal Screening

8. Division of Urology, Tokyo Metropolitan Children’s Medical Center, Tokyo, Japan

9. Japanese Society for Pediatric Urology

10. Japan Endocrine Society

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/31/3/31_2022-0009/_pdf

Reference219 articles.

1. 1. Suwa, S. Nationwide survey of neonatal mass-screening for congenital adrenal hyperplasia in Japan. Screening 1994;3: 141–51.

2. 2. Pang, SY, Wallace, MA, Hofman, L, Thuline, HC, Dorche, C, Lyon, IC, et al. Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Pediatrics 1988;81: 866–74.

3. 3. Suwa, S. Congenital adrenal hyperplasia. Jpn J Pediatr Med 1994;12: 1967–72(in Japanese).

4. 4. Fujieda, K. History of current status of neonatal mass screening for congenital adrenal hyperplasia. Jpn J Pediatr Med 2001;33: 1674–8(in Japanese).

5. 5. Suwa, S, Igarashi, Y, Kitagawa, T, Shimozawa, K, Tsuruhara, T, Matsuura, N, et al. Diagnostic handbook of congenital adrenal hyperplasia (21-hydropxylase deficiency) identified by neonatal mass screening. J Jpn Pediatr Soc 1989;93: 1632–3(in Japanese).

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