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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Detalles Bibliográficos
Autores principales: Bouchireb, Karim, Boyer, Olivia, Mansour-Hendili, Lamisse, Garnier, Arnaud, Heidet, Laurence, Niaudet, Patrick, Salomon, Remi, Poussou, Rosa Vargas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131229/
https://www.ncbi.nlm.nih.gov/pubmed/25112827
http://dx.doi.org/10.1186/1471-2431-14-201

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131229/
https://www.ncbi.nlm.nih.gov/pubmed/25112827
http://dx.doi.org/10.1186/1471-2431-14-201

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