Mervis Carolyn B
Department of Psychological and Brain Sciences, University of Louisville.
Top Lang Disord. 2009 Apr;29(2):149-169. doi: 10.1097/TLD.0b013e3181a72044.
Children with Williams syndrome, a rare neurodevelopmental disorder caused by deletion of ~25 genes on chromosome 7q11.23, evidence large individual differences in both broad language and reading abilities. Nevertheless, as a group, children with this syndrome show a consistent pattern characterized by relative strengths in concrete vocabulary and phonological processing (language skills strongly related to single-word reading) and relative weaknesses in relational concepts, receptive grammar, verbal working memory, comprehension monitoring, and discourse (language skills strongly related to reading comprehension). Children with Williams syndrome who have been taught reading using a systematic phonics approach both decode and comprehend significantly better than children who have been taught using a whole-word approach. Consideration of these patterns in the context of what is known about the reading development of children in the general population provides a strong foundation for facilitating the reading development of children with Williams syndrome.
患有威廉姆斯综合征的儿童,这是一种由7号染色体q11.23区域约25个基因缺失引起的罕见神经发育障碍,在广泛的语言和阅读能力方面存在很大的个体差异。然而,作为一个群体,患有这种综合征的儿童表现出一种一致的模式,其特点是在具体词汇和语音处理方面(与单字阅读密切相关的语言技能)相对较强,而在关系概念、接受性语法、言语工作记忆、理解监控和语篇方面(与阅读理解密切相关的语言技能)相对较弱。使用系统的自然拼读法教授阅读的威廉姆斯综合征儿童在解码和理解方面明显优于使用全词法教授的儿童。在了解普通儿童阅读发展的背景下考虑这些模式,为促进威廉姆斯综合征儿童的阅读发展提供了坚实的基础。