低钙尿
低镁血症
低钾血症
医学
吉特尔曼综合征
代谢性碱中毒
内科学
巴特综合征
噻嗪
远曲小管
内分泌学
醛固酮增多症
代谢紊乱
肾小管病变
血压
肾脏疾病
重吸收
肾
醛固酮
材料科学
镁
冶金
作者
Hans Schepkens,Norbert Lameire
摘要
In 1966, Gitelman described a benign variant of classical Bartter's syndrome in adults characterized by consistent hypomagnesemia and hypocalciuria, hypokalemic metabolic alkalosis and hyperreninemic hyperaldosteronism with normal blood pressure. A specific gene has been found responsible for this disorder, encoding the thiazide-sensitve Na-Cl coporter (TSC) in the distal convoluted tubule. Mutant alleles result in loss of normal TSC function and the phenotype is identical to patients with chronic use of thiazide diuretics. Gitelman's syndrome is a more common cause of chronic hypokalemia than Bartter's syndrome, with which it is often confused. The distinguishing features between both syndromes are discussed.
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