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Verbal Dyspraxia: A Case Study
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作者 Eirini Konstantopoulou Maria Trapali 《Open Journal of Preventive Medicine》 CAS 2023年第1期1-10,共10页
Introduction: While approaching the aspect of learning disorders, particular attention is paid to verbal dyspraxia, a phenomenon that runs its course regularly over the last years. Verbal dyspraxia is inherent in the ... Introduction: While approaching the aspect of learning disorders, particular attention is paid to verbal dyspraxia, a phenomenon that runs its course regularly over the last years. Verbal dyspraxia is inherent in the person without mental disorders and accompanies them throughout the whole spectrum of life. Comorbidity is an added issue. Although dyspraxia is met in homogeneous groups, some common elements such as intelligence, difficulty regarding linguistic skills, low learning performance and low self-esteem are present. Purpose: The object is to research how dyspraxia is manifested and how it affects a 6-year-old boy as well as the possibility of promptly interfering and simplifying his everyday life. Method: In the current case study, Achenbach’s questionnaire was used, combined with the use of expressive vocabulary. Results: The results of the research were unveiled through experts’ references in coordinance with the conferences conducted. Conclusion: Winding up, dyspraxia is a learning disorder that exists within the person through their lifespan. Immediate diagnosis, combined with experts’ personalized intervention programs (and perhaps, a differentiated curriculum, where applicable) can guide the person to live up to the educational needs. Family’s role is to be supportive, intending to eliminate possible emotional strains. 展开更多
关键词 Learning Disorders verbal dyspraxia DIAGNOSIS INTERVENTION Case Study
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Foxp2小鼠模型中发育性言语障碍的分子遗传学研究 被引量:1
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作者 李慧 《实验动物与比较医学》 CAS 2019年第4期331-336,共6页
叉头框P2基因(FOXP2)是第一例发现的与一种特异性言语和语言障碍,即发育性言语失用症相关的基因。这一发现开启了研究相关神经通路的崭新方向。FOXP2在各种脊椎动物中显示了序列和神经系统表达的显著高度保守性,例如它在人胎脑中与对等... 叉头框P2基因(FOXP2)是第一例发现的与一种特异性言语和语言障碍,即发育性言语失用症相关的基因。这一发现开启了研究相关神经通路的崭新方向。FOXP2在各种脊椎动物中显示了序列和神经系统表达的显著高度保守性,例如它在人胎脑中与对等阶段的小鼠胎脑中表达模式高度相似。Foxp2小鼠模型包括基因敲除鼠,类似KE家族病理突变的鼠以及Foxp2被人源化的鼠。本文将从分子网络、感觉处理、运动技能学习等三方面综述对Foxp2小鼠模型的研究,以阐明语言障碍的遗传基础。 展开更多
关键词 叉头框P2基因(FOXP2) 发育性言语失用症 Foxp2小鼠模型 神经通路
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