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Long-term Follow up of Congenital Adrenal Hyperplasia Patients with Hyponatremia
Congenital adrenal hyperplasia (CAH) caused by 21-hydroxylase deficiency is an autosomal recessive disease, which leads to cortisol and aldosterone deficiency and hyperandrogenism. Typical medical treatment includes oral glucocorticoid and mineralocorticoid administration to suppress adrenal androge...
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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
The Korean Society of Electrolyte and Blood Pressure Research
2007
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3894515/ https://ncbi.nlm.nih.gov/pubmed/24459514 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5049/EBP.2007.5.2.140 |
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