A novel compound heterozygous variant of the SLC12A3 gene in Gitelman syndrome with diabetes and the choices of the appropriate hypoglycemic drugs: a case report

BACKGROUND: Gitelman syndrome (GS) is an autosomal recessive tubulopathy caused by mutations of the SLC12A3 gene. It is characterized by hypokalemic metabolic alkalosis, hypomagnesemia and hypocalciuria. It is universally known that both hypokalemia and hypomagnesemia can influence insulin secretion...

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Detalles Bibliográficos
Autores principales: Liu, Zhiying, Wang, Sai, Zhang, Ruixiao, Wang, Cui, Lu, Jingru, Shao, Leping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8336329/
https://www.ncbi.nlm.nih.gov/pubmed/34348722
http://dx.doi.org/10.1186/s12920-021-01047-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8336329/
https://www.ncbi.nlm.nih.gov/pubmed/34348722
http://dx.doi.org/10.1186/s12920-021-01047-1

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