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首页> 外文期刊>PACE: Pacing and clinical electrophysiology >Channelopathies in children and adults.
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Channelopathies in children and adults.

机译:儿童和成人的通道病。

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摘要

In the last decade, pediatric cardiologists have witnessed a revolution in the knowledge of the pathophysiology of rare arrhythmias. The identification of the molecular basis of several hereditary arrhythmia syndromes has been instrumental in this development. Within 12 years the number of causal genes has increased from two in 1995 to at least 24 early 2007 (Table I). Based on this knowledge, established treatment strategies in the 1990s have been modified during the most recent years. This leads to timely and tailored treatment of (asymptomatic) gene carriers, both through personalized lifestyle advices and pharmacologically. At the same time and of equal importance, unaffected family members (noncarriers) can be reassured.
机译:在过去的十年中,儿科心脏病学家目睹了罕见心律失常的病理生理学知识的一场革命。几种遗传性心律不齐综合症的分子基础的鉴定已在这一发展中发挥了作用。在12年内,因果基因的数量已从1995年的2个增加到2007年初的至少24个(表I)。基于这些知识,最近几年对1990年代确立的治疗策略进行了修改。通过个性化的生活方式建议和药理学,这导致对(无症状的)基因携带者进行及时和量身定制的治疗。同时,同样重要的是,未受影响的家庭成员(非承运人)可以放心。

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