Systemic Pseudohypoaldosteronism Type I: A Case Report and Review of the Literature

Systemic pseudohypoaldosteronism (PHA) type I is a rare genetic disorder resulting from mutations in the subunits of the epithelial sodium channel that manifests as severe salt wasting, hyperkalemia, and metabolic acidosis in infancy. In this article we report a patient with systemic PHA type I pres...

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Detalles Bibliográficos
Autores principales: Nur, Nasifa, Lang, Cameron, Hodax, Juanita K., Quintos, Jose Bernardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412170/
https://www.ncbi.nlm.nih.gov/pubmed/28484659
http://dx.doi.org/10.1155/2017/7939854

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412170/
https://www.ncbi.nlm.nih.gov/pubmed/28484659
http://dx.doi.org/10.1155/2017/7939854

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