A case of hypokalemia and proteinuria with a new mutation in the SLC12A3 Gene

BACKGROUND: Gitelman syndrome is an autosomal recessive inherited renal disorder characterized by hypokalemia, hypomagnesemia, and hypocalciuria. Since the symptoms are not severe and laboratory results are not always clear, Gitelman syndrome can go unnoticed by physicians. Here, we report our exper...

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Detalles Bibliográficos
Autores principales: Chen, Qin, Wu, Yaqin, Zhao, Jingya, Jia, Ying, Wang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6194551/
https://www.ncbi.nlm.nih.gov/pubmed/30340552
http://dx.doi.org/10.1186/s12882-018-1083-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6194551/
https://www.ncbi.nlm.nih.gov/pubmed/30340552
http://dx.doi.org/10.1186/s12882-018-1083-2

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