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...

Descripció completa

Dades bibliogràfiques

Autors principals:	PENG Xiaoyan, CHEN Chaoying, YANG Hongxian, XIA Hua, TU Juan
Format:	Artigo
Idioma:	Chinês
Publicat:	Editorial Office of Journal of Rare Diseases 2024-01-01
Col·lecció:	罕见病研究
Matèries:	bartter syndrome type 1 antenatal bartter syndrome renal dysfunction proteinuria
Accés en línia:	https://jrd.chard.org.cn/article/doi/10.12376/j.issn.2097-0501.2024.01.017
Etiquetes:	Afegir etiqueta Sense etiquetes, Sigues el primer a etiquetar aquest registre!