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The Dorsal Mesenchymal Protrusion and the Pathogenesis of Atrioventricular Septal Defects

机译:背叶间质突出和房室间隔缺损的发病机制

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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.
机译:先天性心脏畸形是出生时发现的最常见的缺陷类型。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人数比其他任何先天性畸形都要多,并且每年在美国死于CHD的儿童几乎是所有形式的儿童期癌症的两倍。房室间隔缺损(AVSD)是先天性心脏畸形,大约影响2000名活产婴儿中的1名。患有AVSD的婴儿通常在出生后不久就需要手术干预。然而,即使在成功的手术之后,这些人通常也要应对终生并发症,最常见的是二尖瓣漏气。近年来,对与AVSDs发病机理有关的分子病因和形态学机制的认识已发生了巨大变化。具体来说,这些研究已将第二个心脏场衍生的结构-背叶间质突出(DMP)的异常发育与这种先天性缺陷的发展联系起来。在这篇综述中,我们将讨论DMP在房室间隔复杂的正常形成和AVSD发病机理中的作用的一些最新见解。

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