A case of Gitelman syndrome with proteinuria

A case of Gitelman syndrome with proteinuria

<正>Gitelman综合征(Gitelman syndrome,GS)是一种常染色体隐性遗传性肾小管疾病,主要临床表现为顽固性低钾血症、低镁血症、低尿钙、低氯性碱中毒、血压正常或偏低,继发性肾素-血管紧张素-醛固酮系统(RAAS)激活,该病由Gitelman于1966年首次发现,病因为编码肾远曲小管上皮细胞上的噻嗪类敏感性Na+/Cl-协同转运体(Na+/Cl- cotransporter,NCCT)基因突变所致,部分患者肾脏活检可见肾小球...

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Bibliographic Details
Main Authors: ZHANG Xue, WEI Yi, NIU Yao, CHEN Shan-shan, DU Wei, WENG Xiao-gang
Format: Article
Language:zho
Published: Editorial Department of Journal of Clinical Nephrology 2019-01-01
Series:Linchuang shenzangbing zazhi
Subjects:
Gitelman综合征
低钾血症
SLC12A3基因
蛋白尿
Online Access:http://www.lcszb.com/thesisDetails?columnId=57914343&Fpath=home&index=0
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