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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Detalles Bibliográficos
Autores principales: Song, Jun Hyuk, Lee, Kyu Ha, Kim, Sung Do, Cho, Byoung Soo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Electrolyte and Blood Pressure Research 2007
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3894515/
https://www.ncbi.nlm.nih.gov/pubmed/24459514
http://dx.doi.org/10.5049/EBP.2007.5.2.140

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3894515/
https://www.ncbi.nlm.nih.gov/pubmed/24459514
http://dx.doi.org/10.5049/EBP.2007.5.2.140

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