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心脏发育与先天性心脏结构缺陷。

Heart Development and Congenital Structural Heart Defects.

机构信息

Unité de Cardiologie Pédiatrique et Congénitale and Centre de Référence des Malformations Cardiaques Congénitales Complexes (M3C), Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris (AP-HP), 75015 Paris, France.

Université de Paris, 75015 Paris, France.

出版信息

Annu Rev Genomics Hum Genet. 2021 Aug 31;22:257-284. doi: 10.1146/annurev-genom-083118-015012. Epub 2021 Jun 1.

Abstract

Congenital heart disease is the most frequent birth defect and the leading cause of death for the fetus and in the first year of life. The wide phenotypic diversity of congenital heart defects requires expert diagnosis and sophisticated repair surgery. Although these defects have been described since the seventeenth century, it was only in 2005 that a consensus international nomenclature was adopted, followed by an international classification in 2017 to help provide better management of patients. Advances in genetic engineering, imaging, and omics analyses have uncovered mechanisms of heart formation and malformation in animal models, but approximately 80% of congenital heart defects have an unknown genetic origin. Here, we summarize current knowledge of congenital structural heart defects, intertwining clinical and fundamental research perspectives, with the aim to foster interdisciplinary collaborations at the cutting edge of each field. We also discuss remaining challenges in better understanding congenital heart defects and providing benefits to patients.

摘要

先天性心脏病是最常见的出生缺陷,也是胎儿和生命第一年死亡的主要原因。先天性心脏病的广泛表型多样性需要专家诊断和精湛的修复手术。尽管这些缺陷自 17 世纪以来就有描述,但直到 2005 年才采用了国际共识命名法,随后在 2017 年又采用了国际分类法,以帮助更好地管理患者。遗传工程、成像和组学分析的进步在动物模型中揭示了心脏形成和畸形的机制,但大约 80%的先天性心脏病的遗传起源尚不清楚。在这里,我们总结了先天性结构性心脏病的最新知识,将临床和基础研究的观点交织在一起,旨在促进各领域的交叉学科合作。我们还讨论了在更好地理解先天性心脏病和为患者带来益处方面仍然存在的挑战。

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