Timing of hyponatremia development in patients with salt-wasting-type 21-hydroxylase deficiency

Newborn screening (NBS) can detect 21-hydroxylase deficiency (21-OHD), allowing for early treatment initiation. However, many patients present with adrenal crises or hyponatremia at their first visit. Age (in days) of hyponatremia development in infants with salt-wasting (SW)-type 21-OHD remains unc...

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Detalles Bibliográficos
Autores principales: Shima, Rohi, Sawano, Kentaro, Shibata, Nao, Nyuzuki, Hiromi, Sasaki, Sunao, Sato, Hidetoshi, Ogawa, Yohei, Abe, Yuki, Nagasaki, Keisuke, Saitoh, Akihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society for Pediatric Endocrinology 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7348630/
https://www.ncbi.nlm.nih.gov/pubmed/32694886
http://dx.doi.org/10.1297/cpe.29.105

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7348630/
https://www.ncbi.nlm.nih.gov/pubmed/32694886
http://dx.doi.org/10.1297/cpe.29.105

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