Case report: Gitelman syndrome with diabetes: Confirmed by both hydrochlorothiazide test and genetic testing

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. Hypokalemia, hypomagnesemia, and increased renin-angiotensin-aldosterone system (RAAS) activity can cause gl...

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Detalles Bibliográficos
Autores principales: Yang, Luyang, Fan, Jinmeng, Liu, Yunfeng, Ren, Yi, Liu, Zekun, Fu, Hairui, Qi, Hao, Yang, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
4300
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10270490/
https://www.ncbi.nlm.nih.gov/pubmed/37327293
http://dx.doi.org/10.1097/MD.0000000000033959

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10270490/
https://www.ncbi.nlm.nih.gov/pubmed/37327293
http://dx.doi.org/10.1097/MD.0000000000033959

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