Medical Genetics, Pediatric Cardiology, Genetics and Rare Diseases Research Division, Bambino Gesù Pediatric Hospital, Rome, Italy.
Department of Pediatrics, Sapienza University, Rome, Italy.
Clin Genet. 2019 Feb;95(2):268-276. doi: 10.1111/cge.13375. Epub 2018 May 23.
The atrioventricular canal defect (AVCD) is a congenital heart defect (CHD) frequently associated with extracardiac anomalies (75%). Previous observations from a personal series of patients with AVCD and "polydactyly syndromes" showed that the distinct morphology and combination of AVCD features in some of these syndromes is reminiscent of the cardiac phenotype found in heterotaxy, a malformation complex previously associated with functional cilia abnormalities and aberrant Hedgehog (Hh) signaling. Hh signaling coordinates multiple aspects of left-right lateralization and cardiovascular growth. Being active at the venous pole the secondary heart field (SHF) is essential for normal development of dorsal mesenchymal protrusion and AVCD formation and septation. Experimental data show that perturbations of different components of the Hh pathway can lead to developmental errors presenting with partially overlapping manifestations and AVCD as a common denominator. We review the potential role of Hh signaling in the pathogenesis of AVCD in different genetic disorders. AVCD can be viewed as part of a "developmental field," according to the concept that malformations can be due to defects in signal transduction cascades or pathways, as morphogenetic units which may be altered by Mendelian mutations, aneuploidies, and environmental causes.
房室管缺损 (AVCD) 是一种常见的先天性心脏缺损 (CHD),常伴有心脏外畸形 (75%)。既往对一组伴有 AVCD 和“多指畸形综合征”的患者进行的观察发现,这些综合征中某些 AVCD 特征的独特形态和组合类似于在异构性中发现的心脏表型,异构性是一种先前与功能性纤毛异常和 Hedgehog (Hh) 信号异常相关的畸形复杂症。Hh 信号协调着左右侧化和心血管生长的多个方面。作为静脉极的次级心脏场 (SHF) 对于正常的背侧间质突起和 AVCD 的形成和分隔至关重要。实验数据表明,Hh 途径的不同成分的扰动可能导致具有部分重叠表现的发育性错误,而 AVCD 是一个常见的表现。我们综述了 Hh 信号在不同遗传疾病中导致 AVCD 发病机制的潜在作用。根据畸形可能是由于信号转导级联或途径中的缺陷,作为形态发生单位,可能被孟德尔突变、非整倍体和环境因素改变的概念,AVCD 可以被视为“发育场”的一部分。