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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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| Gepubliceerd in: | J Clin Med |
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| Hoofdauteurs: | , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
MDPI
2020
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7700665/ https://ncbi.nlm.nih.gov/pubmed/33238651 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcm9113790 |
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