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一卵双胎儿同患巴特综合征报告

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摘要 巴特综合征(Bartter syndrome,BS)因1962年由Bartter等首先报道了2例出现低钾性代谢性碱中毒,高醛固酮血症,血压正常,肾组织学检查显示肾小球旁器肥大的患者而得名^[1]。BS的发病率据国外统计约为1/10^6^[2],国内尚无相应的流行病学调查资料。现将我院临床诊断罕见的一卯双胎儿同患BS报告如下。
出处 《临床儿科杂志》 CAS CSCD 北大核心 2009年第4期385-386,共2页 Journal of Clinical Pediatrics
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  • 8Jeck N,Konrad M,Peters M,et al.Mutation in the chloride channel gene,CLCNKB,leading to a mixed Bartter-Gitelman phenotype[J].Pediatr Res,2000,48(6):754-758.
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