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pubmed-article:9676402rdf:typepubmed:Citationlld:pubmed
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pubmed-article:9676402pubmed:dateCreated1998-10-22lld:pubmed
pubmed-article:9676402pubmed:abstractTextThe cases of two patients with transient pseudohypoaldosteronism due to an up to this point unrecognized obstructive renal disease are reported. Both girls presented with a severe salt-losing episode in early infancy mimicking congenital adrenal hyperplasia. Extensive endocrinologic work-up revealed markedly elevated plasma-aldosterone levels. Clinical and laboratory data were consistent with transient pseudohypoaldosteronism. Sonographic and radiological investigation showed in both children a vesicoureteral reflux of differing grades. After therapy of the electrolyte-imbalance and recovery, one of the children required surgical treatment of vesicoureteral reflux.lld:pubmed
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pubmed-article:9676402pubmed:authorpubmed-author:FrigoEElld:pubmed
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pubmed-article:9676402pubmed:pagination174-7lld:pubmed
pubmed-article:9676402pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:9676402pubmed:year1998lld:pubmed
pubmed-article:9676402pubmed:articleTitleTransient pseudohypoaldosteronism in obstructive renal disease.lld:pubmed
pubmed-article:9676402pubmed:affiliationDivision of Pediatric Surgery, University of Vienna, Austria/Europe.lld:pubmed
pubmed-article:9676402pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:9676402pubmed:publicationTypeCase Reportslld:pubmed
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