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对改善全球肾脏病预后组织制定的常染色体显性多囊肾病专家共识解读 被引量:2

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摘要 常染色体显性多囊肾病(ADPKD)全球估计有1 200万患者,在肾脏替代治疗病因中排名第4位[1].近年来ADPKD分子遗传学、生物学、疾病诊断和治疗的相关研究取得了较大进展,然而各国在诊断、评估、预防和治疗等方面存在差异,目前尚无被广泛接受的实践指南.2014年底改善全球肾脏病预后组织(kidney disease improving global outcome,KDIGO)召集全球关于ADPKD的多学科临床专家进行热烈讨论,在科学研究、临床诊治及预防保健等方面达成共识。
出处 《中华内科杂志》 CAS CSCD 北大核心 2016年第8期662-664,共3页 Chinese Journal of Internal Medicine
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  • 1Chapman AB, Devuyst O, Eckardt KU, et al. Autosomal- dominant polycystic kidney disease (ADPKD) :executive summary from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference[J]. Kidney Int, 2015,88 ( 1 ) : 17-27.
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