Fanconi syndrome and severe polyuria: an uncommon clinicobiological presentation of a Gitelman syndrome

BACKGROUND: Gitelman syndrome is an autosomal recessive tubulopathy characterized by hypokalemia, hypomagnesemia, metabolic alkalosis and hypocalciuria. The majority of patients do not present with symptoms until late childhood or adulthood, and the symptoms are generally mild. We report here the fi...

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Bibliographische Detailangaben
Hauptverfasser: Bouchireb, Karim, Boyer, Olivia, Mansour-Hendili, Lamisse, Garnier, Arnaud, Heidet, Laurence, Niaudet, Patrick, Salomon, Remi, Poussou, Rosa Vargas
Format: Artigo
Sprache:Inglês
Veröffentlicht: BioMed Central 2014
Schlagworte:
Case Report
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4131229/
https://ncbi.nlm.nih.gov/pubmed/25112827
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2431-14-201
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