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

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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Bibliographic Details
Main Authors:	Nasifa Nur, Cameron Lang, Juanita K. Hodax, Jose Bernardo Quintos
Format:	Article
Language:	English
Published:	Hindawi Limited 2017-01-01
Series:	Case Reports in Pediatrics
Online Access:	http://dx.doi.org/10.1155/2017/7939854

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