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Teaching reading to children with neurofibromatosis type 1: a clinical trial with random assignment to different approaches

机译:对患有神经纤维瘤病的儿童进行阅读教学1:一项随机分配不同方法的临床试验

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摘要

AIM Neurofibromatosis type 1 (NF1) is a genetic disorder with a cognitive profile that includes visual-spatial perception deficits and a high incidence of reading disability. There is a paucity of information about how this cognitively complex population responds to mainstream reading interventions. The clinical trial goals were to determine whether children and adolescents with NF1 and reading deficits (NF+RD) benefit from mainstream remedial reading programs and whether responsiveness varies with differences in program-related visual-spatial demands.
机译:AIM 1型神经纤维瘤病(NF1)是一种遗传性疾病,具有认知特征,包括视觉空间感知缺陷和阅读障碍的高发生率。关于这一认知复杂的人群如何应对主流阅读干预的信息很少。临床试验的目标是确定患有NF1和阅读障碍(NF + RD)的儿童和青少年是否受益于主流的阅读计划,以及响应性是否随与计划相关的视觉空间需求的变化而变化。

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