Bartter syndrome with long-term follow-up: a case report

Bartter syndrome is a rare inherited disease caused by CLCNKB mutation, which results in inactivation of the chloride channel Kb protein. Bartter syndrome is characterized by extreme hypokalemia, hypochloremia, metabolic alkalosis, hyperrenin-induced angiotensinemia, hyperaldosteronemia, and normal...

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Detalles Bibliográficos
Autores principales: Wu, Xueling, Yang, Gang, Chen, Shiyu, Tang, Min, Jian, Shan, Chen, Fuhui, Wu, Xiulin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7705384/
https://www.ncbi.nlm.nih.gov/pubmed/32857947
http://dx.doi.org/10.1177/0300060520947876

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7705384/
https://www.ncbi.nlm.nih.gov/pubmed/32857947
http://dx.doi.org/10.1177/0300060520947876

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