Still seeking the missing patients with familial hypercholesterolemia

D. Ansell
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Abstract

Received: September 04, 2018; Accepted: September 19, 2018; Published: September 24, 2018 In 2013 the European Atherosclerosis panel [1] highlighted the under diagnosis and under treatment of patients with heterozygous familial hypercholesterolaemia (heFH) in most, if not all, European countries. In the UK, NICE recently updated its clinical guideline (CG71) to primary care doctors for screening patients and identifying patients with heFH [2]. Are we any closer to knowing the true prevalence of heFH?
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仍在寻找失踪的家族性高胆固醇血症患者
收稿日期:2018年9月4日;录用日期:2018年9月19日;2013年,欧洲动脉粥样硬化小组[1]强调了在大多数(如果不是全部的话)欧洲国家,杂合子家族性高胆固醇血症(heFH)患者的诊断和治疗不足。在英国,NICE最近更新了初级保健医生筛查和识别heFH患者的临床指南(CG71)[2]。我们是否更接近了解heFH的真实患病率?
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