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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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| Hauptverfasser: | , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
The Japanese Society for Pediatric Endocrinology
2008
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4004826/ https://ncbi.nlm.nih.gov/pubmed/24790370 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1297/cpe.17.95 |
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