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22q11.2缺失综合征患儿的非典型语言特征及发展轨迹

Atypical language characteristics and trajectories in children with 22q11.2 deletion syndrome.

作者信息

Van Den Heuvel Ellen, Manders Eric, Swillen Ann, Zink Inge

机构信息

KU Leuven, Faculty of Medicine, Department of Neurosciences, Research Group Experimental Oto-Rhino-Laryngology (ExpORL), Herestraat 49 box 721, B-3000 Leuven, Belgium; University Hospitals Leuven, Campus Sint-Rafaël, Department of Oto-Rhino-Laryngology, Head & Neck Surgery, MUCLA, Herestraat 49, B-3000 Leuven, Belgium.

KU Leuven, Faculty of Medicine, Department of Neurosciences, Research Group Experimental Oto-Rhino-Laryngology (ExpORL), Herestraat 49 box 721, B-3000 Leuven, Belgium.

出版信息

J Commun Disord. 2018 Sep-Oct;75:37-56. doi: 10.1016/j.jcomdis.2018.06.001. Epub 2018 Jun 5.

Abstract

BACKGROUND

22q11.2 deletion syndrome (22q11.2DS) is a genetic condition associated with a highly variable phenotypic expression. During childhood speech and language deficits are commonly observed. Findings of cross-sectional studies suggest syndrome-specific and changing language profiles, but a longitudinal approach to identify developmental changes is still lacking to date.

AIMS

The present study aimed to delineate language characteristics and trajectories by comparing the performance of Dutch-speaking school-aged children with 22q11.2DS (n = 18) to those of peers with idiopathic intellectual disability (IID, n  = 19) and to those of children with IID and comorbid autism spectrum disorder (IID + ASD, n = 23). The literature shows contradictory findings regarding language comprehension difficulties in children with 22q11.2DS, we focused on the receptive-expressive language discrepancy. Given their relative strength for verbal short-term memory (VSTM) tasks, a fine-grained error categorization was included to elucidate a possible influence of VSTM on the expressive language outcomes. Finally, we suggested that the inability of children with 22q11.2DS to use contextual information could interfere with morphosyntactic measures.

METHODS

All groups (22q11.2DS, IID, and IID + ASD) were matched for nonverbal fluid reasoning (Gf) using the Analogies and Categories subtests of the Snijders-Oomen Nonverbal Intelligence Test or the Matrix Reasoning and Picture Concepts subtests of the Wechsler Preschool and Primary Scale of Intelligence. Several structural language skills were measured using the Clinical Evaluation of Language Fundamentals and Peabody Picture Vocabulary Test. The same instruments were re-administered after 18 to 24 months. A fine-grained error analysis of the Formulating and Recalling Sentences subtests, both measuring expressive syntax, explored factors contributing to expressive language deficits.

RESULTS

In children with 22q11.2DS the relative advantage of receptive over expressive language had decreased compared to children with IID. For children with 22q11.2DS, complex sentence comprehension remained very challenging over time. Expressive language skills seemed less limited compared to children with IID, and were accompanied by less VSTM difficulties. In children with 22q11.2DS and children with IID + ASD, variable patterns of strengths and weaknesses were demonstrated, resulting in subtle differences between these groups. Error analyses indicated disregard of content-contextual cues and use of vague and elliptic language as being typical for children with 22q11.2DS.

CONCLUSIONS

We recommend that in children with 22q11.2DS the impact of the receptive language impairment should be comprehensively examined and followed-up since it can have a negative effect on their social communication skills, adaptive functioning and academic achievement. Error analysis underscores that multiple measures should be used to evaluate the child's expressive language ability. Further research should focus on developmental trajectories of social communication skills and on the use of intervention strategies to improve language comprehension and pragmatics in school-aged children with 22q11.2DS.

摘要

背景

22q11.2缺失综合征(22q11.2DS)是一种与高度可变表型表达相关的遗传疾病。在儿童期,言语和语言缺陷很常见。横断面研究结果表明存在综合征特异性且不断变化的语言特征,但迄今为止仍缺乏纵向研究方法来确定发育变化情况。

目的

本研究旨在通过比较讲荷兰语的学龄儿童中22q11.2DS患者(n = 18)与特发性智力障碍(IID,n = 19)同龄人以及患有IID和共病自闭症谱系障碍(IID + ASD,n = 23)儿童的表现,来描绘语言特征和轨迹。文献显示关于22q11.2DS儿童语言理解困难的研究结果相互矛盾,我们重点关注接受性 - 表达性语言差异。鉴于他们在言语短期记忆(VSTM)任务方面的相对优势,纳入了细致的错误分类以阐明VSTM对表达性语言结果的可能影响。最后,我们认为22q11.2DS儿童无法利用上下文信息可能会干扰形态句法测量。

方法

使用斯尼德斯 - 奥门非言语智力测验的类比和分类子测验或韦氏学前和小学智力量表的矩阵推理和图片概念子测验,使所有组(22q11.2DS、IID和IID + ASD)在非言语流体推理(Gf)方面相匹配。使用语言基本能力临床评估和皮博迪图片词汇测验测量多种结构语言技能。在18至24个月后重新使用相同工具进行测试。对测量表达性句法的造句和回忆句子子测验进行细致的错误分析,以探究导致表达性语言缺陷的因素。

结果

与IID儿童相比,22q11.2DS儿童接受性语言相对于表达性语言的相对优势有所下降。对于22q11.2DS儿童,随着时间推移,复杂句子理解仍然极具挑战性。与IID儿童相比,表达性语言技能似乎受限较小,且伴随的VSTM困难也较少。在22q11.2DS儿童和IID + ASD儿童中,表现出优势和劣势的可变模式,导致这些组之间存在细微差异。错误分析表明,忽视内容上下文线索以及使用模糊和省略语言是22q11.2DS儿童的典型特征。

结论

我们建议,对于22q11.2DS儿童,应全面检查并跟踪接受性语言障碍的影响,因为它可能对他们的社会沟通技能、适应性功能和学业成绩产生负面影响。错误分析强调应使用多种测量方法来评估儿童的表达性语言能力。进一步的研究应侧重于社会沟通技能的发展轨迹以及使用干预策略来改善22q11.2DS学龄儿童的语言理解和语用能力。

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