Cortical Vision Impairment (CVI)-informed assessment and treatment of challenging behavior in a child with SCN2A-related disorder.

IF 4.1 2区 医学 Q1 CLINICAL NEUROLOGY
Benjamin R Thomas, Natasha N Ludwig, Danielle Pelletier, Melanie Bauer, Rebecca Hommer, Constance Smith-Hicks, Julia T O'Connor
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引用次数: 0

Abstract

This report presents results of parent-implemented behavioral treatments for a child with cortical visual impairment (CVI), intellectual disability (ID), epilepsy, and autism spectrum disorder (ASD) associated with a pathogenic variant in the SCN2A gene (i.e., SCN2A-Related Disorder). Treatment evaluations were informed by combined results of functional behavior assessment (FBA) and functional vision assessment (FVA) which yielded CVI-related accommodations. The treatment of escape-maintained challenging behavior involved the evaluation of behavioral prompting strategies in accordance with CVI-related accommodations, extinction (EXT), and differential reinforcement modifications. The treatment for behavior problems maintained by access to food (tangible-edible) included functional communication training (FCT), EXT, and schedule thinning with schedule-correlated visual signals. Overall, integrating child-specific CVI-related accommodations was essential for developing effective behavioral interventions for this child. FVAs are accessible and practical for uptake by behavior analysts in vision-informed assessment and treatment of challenging behavior.

皮质性视力障碍(CVI)信息评估和治疗儿童scn2a相关障碍的挑战行为。
本报告介绍了父母实施的行为治疗的结果,儿童皮质视力障碍(CVI),智力残疾(ID),癫痫和自闭症谱系障碍(ASD)与SCN2A基因致病变异(即SCN2A相关障碍)相关。治疗评估采用功能行为评估(FBA)和功能视觉评估(FVA)的综合结果,得出与cvi相关的调整。逃避维持挑战行为的治疗包括根据cvi相关调节、消退(EXT)和差异强化修改来评估行为提示策略。通过获取食物(有形-可食用)来维持行为问题的治疗包括功能性沟通训练(FCT)、EXT和使用与时间表相关的视觉信号来减少时间表。总体而言,整合儿童特定的cvi相关住宿对于为该儿童制定有效的行为干预措施至关重要。对于行为分析师来说,在视觉知情的评估和挑战性行为的处理中,fva是可访问的和实用的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.60
自引率
4.10%
发文量
58
审稿时长
>12 weeks
期刊介绍: Journal of Neurodevelopmental Disorders is an open access journal that integrates current, cutting-edge research across a number of disciplines, including neurobiology, genetics, cognitive neuroscience, psychiatry and psychology. The journal’s primary focus is on the pathogenesis of neurodevelopmental disorders including autism, fragile X syndrome, tuberous sclerosis, Turner Syndrome, 22q Deletion Syndrome, Prader-Willi and Angelman Syndrome, Williams syndrome, lysosomal storage diseases, dyslexia, specific language impairment and fetal alcohol syndrome. With the discovery of specific genes underlying neurodevelopmental syndromes, the emergence of powerful tools for studying neural circuitry, and the development of new approaches for exploring molecular mechanisms, interdisciplinary research on the pathogenesis of neurodevelopmental disorders is now increasingly common. Journal of Neurodevelopmental Disorders provides a unique venue for researchers interested in comparing and contrasting mechanisms and characteristics related to the pathogenesis of the full range of neurodevelopmental disorders, sharpening our understanding of the etiology and relevant phenotypes of each condition.
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