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自闭症谱系障碍中的关键突触病理学:遗传机制与最新进展。

Key Synaptic Pathology in Autism Spectrum Disorder: Genetic Mechanisms and Recent Advances.

机构信息

Department of Pathology, Chengdu Women's and Children's Central Hospital, School of Medicine, University of Electronic Science and Technology of China, 611731 Chengdu, Sichuan, China.

Department of Pathology, The Affiliated Hospital, Southwest Medical University, 646000 Luzhou, Sichuan, China.

出版信息

J Integr Neurosci. 2024 Sep 29;23(10):184. doi: 10.31083/j.jin2310184.

Abstract

Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by impaired social interactions and verbal communication, accompanied by symptoms of restricted and repetitive patterns of behavior or interest. Over the past 30 years, the morbidity of ASD has increased in most areas of the world. Although the pathogenesis of ASD is not fully understood, it has been associated with over 1000 genes or genomic loci, indicating the importance and complexity of the genetic mechanisms involved. This review focuses on the synaptic pathology of ASD and particularly on genetic variants involved in synaptic structure and functions. These include , , , , and as well as other potentially novel genes such as , , and that could be core elements in ASD pathogenesis. Here, we summarize several pathological pathways supporting the hypothesis that synaptic pathology caused by genetic mutations may be the pathogenic basis for ASD.

摘要

自闭症谱系障碍(ASD)是一种神经发育障碍,其特征是社交互动和言语交流受损,伴有行为或兴趣受限和重复模式的症状。在过去的 30 年中,ASD 在世界上大多数地区的发病率都有所增加。尽管 ASD 的发病机制尚不完全清楚,但它与超过 1000 个基因或基因组位点有关,这表明所涉及的遗传机制的重要性和复杂性。本篇综述重点介绍 ASD 的突触病理学,特别是涉及突触结构和功能的遗传变异。这些包括 SHANK3、NRXN1、GRIN2A、SLC1A1 和 CNTNAP2 等,以及其他潜在的新基因,如 RELN、IL1RAPL1 和 CCDC88C 等,它们可能是 ASD 发病机制的核心要素。在这里,我们总结了几个支持遗传突变引起的突触病理学可能是 ASD 发病基础的假说的病理途径。

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