低镁血症
医学
低钙尿
吉特尔曼综合征
低钾血症
发病机制
病因学
病理生理学
生物信息学
内科学
生物
材料科学
镁
冶金
标识
DOI:10.1053/j.ackd.2006.01.014
摘要
In the past decade our understanding of the etiology and pathophysiology of Gitelman syndrome, an autosomal recessive salt-losing tubular disorder with secondary hypokalemia, has increased considerably through the achievements of molecular genetics and cell physiology. In this short review, I will summarize the most recent data on the clinical and biochemical phenotype, the molecular causes, and the pathogenesis of Gitelman syndrome. I will especially focus on the recent elucidation of the mechanisms involved in the pathogenesis of the hypomagnesemia and hypocalciuria that accompanies Gitelman syndrome.
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