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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...
Autores principales: | Shima, Rohi, Sawano, Kentaro, Shibata, Nao, Nyuzuki, Hiromi, Sasaki, Sunao, Sato, Hidetoshi, Ogawa, Yohei, Abe, Yuki, Nagasaki, Keisuke, Saitoh, Akihiko |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society for Pediatric Endocrinology
2020
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Materias: | |
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 |
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