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Bartter syndrome type III with glomerular dysplasia and chronic kidney disease: A case report

BACKGROUND: Bartter syndrome (BS) type III is a rare autosomal recessive genetic disease. Its clinical features are polyuria, hypokalemia, hypochloremia, metabolic alkalosis, and hyperreninaemia. A few BS type III can be complicated with chronic kidney disease. CASE PRESENTATION: We report a 14-year...

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Detalles Bibliográficos
Autores principales:	Liu, Jingqi, Zhang, Yudi, Wu, Xiaochuan, Li, Yongzhen
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2023
Materias:	Pediatrics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10098006/ https://www.ncbi.nlm.nih.gov/pubmed/37063660 http://dx.doi.org/10.3389/fped.2023.1169486

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