A call for funds and training for kidney genomics programmes

IF 39.8 1区 医学 Q1 UROLOGY & NEPHROLOGY
Kar Hui Ng
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引用次数: 0

Abstract Image

呼吁为肾脏基因组学项目提供资金和培训
在资源有限的国家,由于无法获得基因检测,导致对遗传性肾病的诊断不足,从而错过了开始治疗以预防肾衰竭的机会。要在这些国家实施肾脏基因组学规划,需要资金、教育和卫生保健工作人员的参与。新加坡是一个被低收入和中等收入国家包围的高收入国家,作为一名对基因组学感兴趣的肾病学家,我在工作中目睹了基因检测方面的差异和不平等。国际指南推荐基因检测用于慢性肾脏疾病和肾小球疾病的诊断评估。然而,在亚洲许多资源有限的地区,由于缺乏获得这种检测的机会,遗传性肾脏疾病未得到充分认识和诊断。单基因肾病占成人慢性肾病的40%,全世界每106人中就有1人,新加坡每150人中就有1人携带可导致阿尔波特综合征的基因变异。
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来源期刊
Nature Reviews Nephrology
Nature Reviews Nephrology 医学-泌尿学与肾脏学
CiteScore
39.00
自引率
1.20%
发文量
127
审稿时长
6-12 weeks
期刊介绍: Nature Reviews Nephrology aims to be the premier source of reviews and commentaries for the scientific communities it serves. It strives to publish authoritative, accessible articles. Articles are enhanced with clearly understandable figures, tables, and other display items. Nature Reviews Nephrology publishes Research Highlights, News & Views, Comments, Reviews, Perspectives, and Consensus Statements. The content is relevant to nephrologists and basic science researchers. The broad scope of the journal ensures that the work reaches the widest possible audience.
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