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年轻人的心源性猝死:一种临床遗传学方法。

Sudden cardiac death in the young: a clinical genetic approach.

作者信息

Ingles J, Semsarian C

机构信息

Agnes Ginges Centre for Molecular Cardiology, Centenary Institute, Sydney, NSW, Australia.

出版信息

Intern Med J. 2007 Jan;37(1):32-7. doi: 10.1111/j.1445-5994.2006.01241.x.

Abstract

The sudden death of a young person is a devastating event for both the family and community. Over the last decade, significant advances have been made in understanding both the clinical and genetic basis of sudden cardiac death in the young. Many of the causes of sudden death in the young are due to genetic heart disorders, which can lead to both structural (e.g. hypertrophic cardiomyopathy) and arrhythmogenic (e.g. familial long QT syndrome) abnormalities. Most commonly, sudden cardiac death in the young can be the first presentation of an underlying heart problem, leaving the family at a loss as to why an otherwise healthy young person has died. Not only is this a tragic event for those involved, but it also presents a medical challenge to the clinician involved in the management of the surviving family members. Evaluation of families requires a multidisciplinary approach, which should include cardiologists, a clinical geneticist, a genetic counsellor and the forensic pathologist directly involved in the sudden death case. This multifaceted cardiac genetic service is crucial in the evaluation and management of the clinical, genetic, psychological and social complexities observed in families in which there has been a young sudden cardiac death.

摘要

年轻人的突然死亡对其家庭和社区来说都是一场毁灭性的事件。在过去十年中,在了解年轻人心脏性猝死的临床和遗传基础方面取得了重大进展。年轻人猝死的许多原因都归因于遗传性心脏疾病,这些疾病可导致结构性异常(如肥厚型心肌病)和致心律失常性异常(如家族性长QT综合征)。最常见的情况是,年轻人心脏性猝死可能是潜在心脏问题的首次表现,这让家人对原本健康的年轻人为何死亡感到困惑。这不仅对相关人员来说是一场悲剧,对于参与幸存家庭成员管理的临床医生而言也是一项医学挑战。对家庭进行评估需要采取多学科方法,其中应包括心脏病专家、临床遗传学家、遗传咨询师以及直接参与猝死病例的法医病理学家。这种多方面的心脏遗传服务对于评估和管理在年轻人心脏性猝死家庭中观察到的临床、遗传、心理和社会复杂性至关重要。

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