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Clinical and Genetic Features in 31 Serial Chinese Children With Gitelman Syndrome

Gitelman syndrome (GS, OMIM 263800) is a genetic congenital tubulopathy associated with salt loss, which is characterized by hypokalemic metabolic toxicity, hypocalciuria, and hypomagnesemia. GS, which is typically detected in adolescence or adulthood, has long been considered a benign tubular lesio...

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Detalles Bibliográficos
Autores principales:	Zhang, Lingxia, Huang, Ke, Wang, Shugang, Fu, Haidong, Wang, Jingjing, Shen, Huijun, Lu, Zhihong, Chen, Junyi, Bao, Yu, Feng, Chunyue, Dong, Guanping, Mao, Jianhua
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2021
Materias:	Pediatrics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8116576/ https://www.ncbi.nlm.nih.gov/pubmed/33996672 http://dx.doi.org/10.3389/fped.2021.544925

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