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Article

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

The Journal of international medical research - 1 Aug 2020

Wu Xueling, Yang Gang, Chen Shiyu, Tang Min, Jian Shan, Chen Fuhui, Wu Xiulin

Abstract excerpt

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 blood pressure. We herein report a case of Bartter syndrome that manifested as vomiting, hypokalemia, metabolic...

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Identifiers

PMID: 32857947
DOI: 10.1177/0300060520947876
PMCID: PMC7705384

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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