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

Internet

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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