Early diagnosis of Gitelman syndrome in a young child: A case report

BACKGROUND: Gitelman syndrome (GS) is an autosomal recessive renal tubular disorder characterized by renal wasting hypokalemia, metabolic alkalosis, hypomagnesemia, and hypocalciuria. It is usually caused by mutations in the gene SLC12A3, which encodes the thiazide-sensitive Na-Cl cotransporter. GS...

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Detalles Bibliográficos
Autores principales: Wu, Chun-Yen, Tsai, Ming-Hsein, Chen, Chia-Chun, Kao, Chuan-Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8968817/
https://www.ncbi.nlm.nih.gov/pubmed/35434103
http://dx.doi.org/10.12998/wjcc.v10.i9.2844

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8968817/
https://www.ncbi.nlm.nih.gov/pubmed/35434103
http://dx.doi.org/10.12998/wjcc.v10.i9.2844

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