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Investigation of Vestibular Function in Adult Patients with Gitelman Syndrome: Results of an Observational Study

Gitelman syndrome (GS) is a rare salt-losing tubulopathy caused by an inactivating mutation in the SLC12A3 gene, encoding the thiazide-sensitive sodium chloride cotransporter (NCC). Patients with GS frequently complain of vertigo, usually attributed to hypovolemia. Because NCC is also located in the...

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Detalles Bibliográficos
Autores principales:	Alexandru, Mihaela, Courbebaisse, Marie, Le Pajolec, Christine, Ménage, Adeline, Papon, Jean-François, Vargas-Poussou, Rosa, Nevoux, Jérôme, Blanchard, Anne
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2020
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7700665/ https://www.ncbi.nlm.nih.gov/pubmed/33238651 http://dx.doi.org/10.3390/jcm9113790

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