摘要
遗传学研究进入后基因组时代以来,语言障碍的高遗传度已被证实。多种基因相关疾病均可能导致成人或儿童表现出不同程度的语言障碍。综述探讨了近十年来发现的较为常见的语言障碍疾病及其生物学机制,梳理了阅读障碍、额颞叶变性、特定型语言障碍、儿童言语失用症等与语言障碍密切相关的单一疾病的基因研究,以及对多种疾病共同的基因的探讨,以期揭示语言障碍的基因关联或致病机理,为语言障碍的预防及诊疗提供线索。
Since genetic research entered the post-genomic era,the high heritability of language disorders has been confirmed.A variety of genetic-related diseases may cause various types of language disorders in children and/or adults.This article has summarized language disorders and their underlying mechanisms by searching the Web of Science database over the last decade,and combed the genetic researches for dyslexia,frontotemporal degeneration,specific language disorder,childhood speech apraxia and other single diseases that are strongly associated with the language disorders.It also provided a discussion over the co-occurrence of multiple diseases,with an aim to revealing the genetic association and/or pathogenetic mechanism in order to provide inspiration for the prevention,diagnosis,and treatment of language disorders.
作者
王霞
潘雪瑶
李西
姜孟
Wang Xia;Pan Xueyao;Li Xi;Jiang Meng(School of English Studies/Language Brain&Research Center,Sichuan International Studies University,Chongqing 400031,China;College of Language Intelligence/Language Brain&Research Center,Sichuan International Studies University,Chongqing 400031,China)
出处
《中华医学遗传学杂志》
CAS
CSCD
2024年第3期377-382,共6页
Chinese Journal of Medical Genetics
基金
重庆市社科规划一般项目(2019YBYY131)
四川外国语大学重点项目(sisu202002)。
关键词
阅读障碍
额颞叶变性
特定型语言障碍
儿童言语失用症
基因
Dyslexia
Frontotemporal degeneration
Specific language disorder
Childhood speech apraxia
Gene