Cargando…
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...
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: | |
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 |
Ejemplares similares
-
Long-Term Outcomes of Congenital Adrenal Hyperplasia
por: Nordenström, Anna, et al.
Publicado: (2022) -
Long term follow up of growth in children with Congenital Adrenal Hyperplasia 21- Hydroxylase deficiency
por: Parikh, Ruchi, et al.
Publicado: (2015) -
Long-term follow-up of a female with congenital adrenal hyperplasia due to P450-oxidoreductase deficiency
por: Bonamichi, Beatriz D. S. F., et al.
Publicado: (2016) -
Long-term treatment of a child with congenital adrenal hyperplasia
por: Pratignyo, Rogatianus Bagus, et al.
Publicado: (2013) -
Congenital adrenal hyperplasia
por: Dessinioti, Cleo, et al.
Publicado: (2009)