口腔颌面裂隙的新见解:意大利样本的流行病学和遗传学研究

New insights in orofacial cleft: epidemiological and genetic studies on italian samples.

作者信息

Tettamanti L, Avantaggiato A, Nardone M, Palmieri A, Tagliabue A

机构信息

Department of Medicine and Surgery, University of Insubria, Varese, Italy.

Department of Morphology, Surgery and Experimental Medicine, University of Ferrara, Ferrara, Italy.

出版信息

Oral Implantol (Rome). 2017 Apr 10;10(1):11-19. doi: 10.11138/orl/2017.10.1.011. eCollection 2017 Jan-Mar.

Abstract

Cleft of the lip and/or palate (CL±P) is the most common congenital craniofacial anomaly affecting around 1 in 700 live births worldwide. Clefts of the human face can be classified anatomically as cleft lip only (CL), cleft palate only (CP), cleft lip and palate (CLP) or a combined group of cleft lip with or without cleft palate (CL±P), based on differences in embryologic development. CL±P has a genetic base and several linkage and association analyses have been performed in order to obtain important information about the role of candidate genes in its onset; not less important are gene-environment interactions that play an increasing role in its aetiology. In CL±P, several loci have been seen associated with the malformation, and, in some cases, a specific gene mapping in a locus has also been identified as susceptibility factor. In CP, one gene has been found, but many more are probably involved. In this short review the genetic studies carried out on CL±P, and the interaction with environmental factors (alcohol, smoking, drugs) are discussed.

摘要

唇裂和/或腭裂(CL±P)是最常见的先天性颅面畸形,全球每700例活产婴儿中约有1例受其影响。根据胚胎发育差异,人类面部的裂隙在解剖学上可分为单纯唇裂(CL)、单纯腭裂(CP)、唇腭裂(CLP)或伴有或不伴有腭裂的唇裂组合(CL±P)。CL±P具有遗传基础,已经进行了多项连锁和关联分析,以获取有关候选基因在其发病中作用的重要信息;基因-环境相互作用在其病因学中发挥着越来越重要的作用,这一点同样重要。在CL±P中,已发现多个基因座与该畸形相关,在某些情况下,位于一个基因座上的特定基因图谱也已被确定为易感因素。在CP中,已发现一个基因,但可能还有更多基因与之相关。在这篇简短的综述中,我们讨论了对CL±P进行的遗传学研究以及与环境因素(酒精、吸烟、药物)的相互作用。

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