Prenatal Diagnosis and Treatment of Steroid 21-Hydroxylase Deficiency

Steroid 21-hydroxylase deficiency (21-OHD) accounts for 90–95% of congenital adrenal hyperplasia (CAH) cases. It is classified into three distinct clinical phenotypes: the salt-wasting (SW), simple virilizing (SV) and nonclassical forms (NC). As girls with the SW and SV forms of 21-OHD are exposed t...

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Detalles Bibliográficos
Autores principales: Tajima, Toshihiro, Fujieda, Kenji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society for Pediatric Endocrinology 2008
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4004826/
https://www.ncbi.nlm.nih.gov/pubmed/24790370
http://dx.doi.org/10.1297/cpe.17.95

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4004826/
https://www.ncbi.nlm.nih.gov/pubmed/24790370
http://dx.doi.org/10.1297/cpe.17.95

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