Cargando…
Critical Points in the Management of Pseudohypoaldosteronism Type 1
Pseudohypoaldosteronism type 1 (PHA-1, MIM #264350) is caused by defective transepithelial sodium transport. Affected patients develop life-threatening neonatal-onset salt loss, hyperkalemia, acidosis, and elevated aldosterone levels due to end-organ resistance to aldosterone. In this report, we pre...
Autores principales: | Güran, Tülay, Değirmenci, Serpil, Bulut, İpek K., Say, Aysun, Riepe, Felix G., Güran, Ömer |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Galenos Publishing
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3119449/ https://www.ncbi.nlm.nih.gov/pubmed/21750640 http://dx.doi.org/10.4274/jcrpe.v3i2.20 |
Ejemplares similares
-
A Giant Ovarian Cyst in a Neonate with Classical 21-Hydroxylase Deficiency with Very High Testosterone Levels Demonstrating a High-Dose Hook Effect
por: Güran, Tülay, et al.
Publicado: (2012) -
Phenotypic variation of autosomal recessive pseudohypoaldosteronism type I: a case in point
por: Kala Ahluwalia, Gunjeet, et al.
Publicado: (2014) -
Latest Insights on the Etiology and Management of Primary Adrenal Insufficiency in Children
por: Güran, Tülay
Publicado: (2017) -
Dermal and Ophthalmic Findings in Pseudohypoaldosteronism
por: Korkut, Sabriye, et al.
Publicado: (2015) -
Systemic Pseudohypoaldosteronism Type I: A Case Report and Review of the Literature
por: Nur, Nasifa, et al.
Publicado: (2017)