Bartter-Like Syndrome as the Initial Presentation of Dent Disease 1: A Case Report

Dent disease is a rare genetic disease characterized by low-molecular-weight proteinuria. Dent disease with Bartter-like syndrome is rare and can easily be misdiagnosed and mistreated. Herein, we report a case of Dent disease 1 with Bartter-like syndrome as the initial manifestation. The patient was...

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Detalles Bibliográficos
Autores principales: Chen, Qiaoping, Cao, Yan, Xu, Liyun, Liu, Jingqi, Wu, Xiaochuan
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/PMC8506038/
https://www.ncbi.nlm.nih.gov/pubmed/34650943
http://dx.doi.org/10.3389/fped.2021.725251

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8506038/
https://www.ncbi.nlm.nih.gov/pubmed/34650943
http://dx.doi.org/10.3389/fped.2021.725251

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