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

Congenital adrenal hyperplasia is a category of disorders characterized by impaired adrenocortical steroidogenesis. The most frequent disorder of congenital adrenal hyperplasia is 21-hydroxylase deficiency, which is caused by pathogenic variants of CAY21A2 and is prevalent between 1 in 18,000 and 20...

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Detalles Bibliográficos
Autores principales: Ishii, Tomohiro, Kashimada, Kenichi, Amano, Naoko, Takasawa, Kei, Nakamura-Utsunomiya, Akari, Yatsuga, Shuichi, Mukai, Tokuo, Ida, Shinobu, Isobe, Mitsuhisa, Fukushi, Masaru, Satoh, Hiroyuki, Yoshino, Kaoru, Otsuki, Michio, Katabami, Takuyuki, Tajima, Toshihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society for Pediatric Endocrinology 2022
Materias:
Special Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9297175/
https://www.ncbi.nlm.nih.gov/pubmed/35928387
http://dx.doi.org/10.1297/cpe.2022-0009

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9297175/
https://www.ncbi.nlm.nih.gov/pubmed/35928387
http://dx.doi.org/10.1297/cpe.2022-0009

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