Spontaneous Coronary Artery Dissection as Presenting Feature of Vascular Ehlers-Danlos Syndrome

IF 0.5 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Cardiogenetics Pub Date : 2021-08-13 DOI:10.3390/cardiogenetics11030014
J. Bos, E. Overwater, M. Dirksen, S. Şimşek, S. Demirdas, A. Houweling
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引用次数: 0

Abstract

A spontaneous coronary artery dissection as the sole presenting feature of vascular Ehlers-Danlos syndrome is an uncommon finding. We present a 33-year-old woman with sudden onset chest pain caused by a spontaneous coronary artery dissection. Genetic testing revealed vascular Ehlers-Danlos syndrome as the underlying cause. Specifically, we show the value of genetic testing, which in some patients may be the only way of establishing a diagnosis.
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自发性冠状动脉剥离是血管性埃勒-丹洛斯综合征的表现特征
自发性冠状动脉剥离作为血管型埃勒-丹洛斯综合征的唯一表现特征是一种罕见的发现。我们提出一个33岁的妇女突发胸痛引起的自发性冠状动脉夹层。基因检测显示血管性埃勒-丹洛斯综合征是潜在的病因。具体来说,我们展示了基因检测的价值,这在一些患者中可能是建立诊断的唯一方法。
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来源期刊
Cardiogenetics
Cardiogenetics CARDIAC & CARDIOVASCULAR SYSTEMS-
自引率
0.00%
发文量
26
审稿时长
11 weeks
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