Olson R, Wise B, Conners F, Rack J, Fulker D
J Learn Disabil. 1989 Jun-Jul;22(6):339-48. doi: 10.1177/002221948902200604.
Phonological coding, measured by the oral reading of nonwords, and orthographic coding, measured by the discrimination of words from homophonic nonwords (e.g., rane, rain), were compared for pairs of older children with reading disabilities (RD) and younger nondisabled readers matched on word recognition. Phonological coding was substantially lower for most children with RD, indicating a unique developmental deficit in phonological coding rather than an equal developmental lag across all component reading skills. Data from identical and fraternal twins indicated that the phonological coding deficit of the children with RD was highly heritable and accounted for most of the heritable variance in their word recognition deficits. The deficits of the twins with RD in segmental language skills (rhyming and phoneme segmentation) were related to the heritable variance in their phonological coding deficits. Orthographic coding was not significantly heritable, and it accounted for much of the environmental variance in word recognition deficits. Implications of the results for the remediation of reading disability are discussed.
通过对非词进行口头朗读来衡量的语音编码,以及通过区分单词与同音非词(如rane、rain)来衡量的正字法编码,在年龄较大的阅读障碍(RD)儿童与在单词识别方面匹配的较年轻的非阅读障碍读者对之间进行了比较。大多数患有阅读障碍的儿童的语音编码明显较低,这表明语音编码存在独特的发育缺陷,而不是所有阅读技能成分都存在同等的发育滞后。来自同卵双胞胎和异卵双胞胎的数据表明,患有阅读障碍的儿童的语音编码缺陷具有高度遗传性,并且占其单词识别缺陷中大部分可遗传变异。患有阅读障碍的双胞胎在片段语言技能(押韵和音素分割)方面的缺陷与他们语音编码缺陷中的可遗传变异有关。正字法编码没有显著的遗传性,并且它占单词识别缺陷中大部分环境变异。讨论了这些结果对阅读障碍补救的意义。