A Case of Childhood-Onset Bartter Syndrome Type 1 with Renal Dysfunction

A Case of Childhood-Onset Bartter Syndrome Type 1 with Renal Dysfunction

Bartter syndrome (BS, OMIM #601678) is a rare inherited salt-losing tubulopathy characterized by hypokalemia metabolic alkalosis with secondary renin-angiotensin-aldosterone system activation. As reported, BS type 1 is generally presented prenatal and neonatal period, and symptoms usually appear bef...

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Bibliographic Details
Main Authors: PENG Xiaoyan, CHEN Chaoying, YANG Hongxian, XIA Hua, TU Juan
Format: Article
Language:zho
Published: Editorial Office of Journal of Rare Diseases 2024-01-01
Series:罕见病研究
Subjects:
bartter syndrome type 1
antenatal bartter syndrome
renal dysfunction
proteinuria
Online Access:https://jrd.chard.org.cn/article/doi/10.12376/j.issn.2097-0501.2024.01.017

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https://jrd.chard.org.cn/article/doi/10.12376/j.issn.2097-0501.2024.01.017

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