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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Main Authors: Bouchireb, Karim, Boyer, Olivia, Mansour-Hendili, Lamisse, Garnier, Arnaud, Heidet, Laurence, Niaudet, Patrick, Salomon, Remi, Poussou, Rosa Vargas
Formato: Artigo
Idioma:Inglês
Publicado: BioMed Central 2014
Assuntos:
Case Report
Acceso en liña: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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