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背侧间充质突出与房室间隔缺损的发病机制

The Dorsal Mesenchymal Protrusion and the Pathogenesis of Atrioventricular Septal Defects.

作者信息

Burns Tara, Yang Yanping, Hiriart Emilye, Wessels Andy

机构信息

Department of Regenerative Medicine and Cell Biology, Medical University of South Carolina, 173 Ashley Avenue, Charleston, SC 29425, USA.

Department of Regenerative Medicine and Cell Biology, Medical University of South Carolina, 173 Ashley Avenue, Charleston, SC 29425, USA; Department of Histology and Embryology, Shanxi Medical University, No 56 Xin Jian Nan Road, Taiyuan 030001, Shanxi, China.

出版信息

J Cardiovasc Dev Dis. 2016 Dec;3(4). doi: 10.3390/jcdd3040029. Epub 2016 Sep 26.

Abstract

Congenital heart malformations are the most common type of defects found at birth. About 1% of infants are born with one or more heart defect on a yearly basis. Congenital Heart Disease (CHD) causes more deaths in the first year of life than any other congenital abnormality, and each year, nearly twice as many children die in the United States from CHD as from all forms of childhood cancers combined. Atrioventricular septal defects (AVSD) are congenital heart malformations affecting approximately 1 in 2000 live births. Babies born with an AVSD often require surgical intervention shortly after birth. However, even after successful surgery, these individuals typically have to deal with lifelong complications with the most common being a leaky mitral valve. In recent years the understanding of the molecular etiology and morphological mechanisms associated with the pathogenesis of AVSDs has significantly changed. Specifically, these studies have linked abnormal development of the Dorsal Mesenchymal Protrusion (DMP), a Second Heart Field-derived structure, to the development of this congenital defect. In this review we will be discuss some of the latest insights into the role of the DMP in the normal formation of the atrioventricular septal complex and in the pathogenesis of AVSDs.

摘要

先天性心脏畸形是出生时最常见的缺陷类型。每年约有1%的婴儿出生时患有一种或多种心脏缺陷。先天性心脏病(CHD)在生命的第一年导致的死亡比任何其他先天性异常都多,在美国,每年死于CHD的儿童数量几乎是死于所有形式儿童癌症的两倍。房室间隔缺损(AVSD)是一种先天性心脏畸形,每2000例活产中约有1例受影响。患有AVSD的婴儿通常在出生后不久就需要手术干预。然而,即使手术成功,这些人通常也必须应对终身并发症,最常见的是二尖瓣反流。近年来,对与AVSD发病机制相关的分子病因和形态学机制的认识发生了显著变化。具体而言,这些研究将背侧间充质突出(DMP)(一种源自第二心脏场的结构)的异常发育与这种先天性缺陷的发生联系起来。在这篇综述中,我们将讨论DMP在房室间隔复合体正常形成以及AVSD发病机制中的作用的一些最新见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aab3/5715722/95a64ecf5c54/jcdd-03-00029-g001.jpg

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