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首页> 外文期刊>American Journal of Physiology >Subepicardial phase 0 block and discontinuous transmural conduction underlie right precordial ST-segment elevation by a SCN5A loss-of-function mutation
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Subepicardial phase 0 block and discontinuous transmural conduction underlie right precordial ST-segment elevation by a SCN5A loss-of-function mutation

机译:心外膜下0期阻滞和不连续的透壁传导是SCN5A功能丧失突变导致右心前区ST段抬高的基础

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摘要

Two mechanisms are generally proposed to explain right precordial ST-segment elevation in Brugada syndrome: 1) right ventricular (RV) subepicardial action potential shortening and/or loss of dome causing transmural dispersion of repolarization; and 2) RV conduction delay. Here we report novel mechanistic insights into ST-segment elevation associated with a Na~+ current (I_(Na)) loss-of-function mutation from studies in a Dutch kindred with the COOH-terminal SCN5A variant p.Phe2004Leu. The proband, a man, experienced syncope at age 22 yr and had coved-type ST-segment elevations in ECG leads VI and V2 and negative T waves in V2.
机译:提出了两种机制来解释Brugada综合征的右心前区ST段抬高:1)右心室(RV)心外膜下动作电位缩短和/或穹顶丢失,引起跨膜性复极分散。 2)RV传导延迟。在这里,我们从与荷兰人一起进行的带有COOH末端SCN5A变体p.Phe2004Leu的研究中报告了与Na〜+电流(I_(Na))功能丧失突变相关的ST段抬高的新机制。先证者,一名男子,在22岁时经历了晕厥,心电图VI和V2导联的ST段抬高呈弓形,而V2导联的T呈负向。

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