Chromosomal translocation in a child with SLI and apraxia.

L Weistuch, N B Schiff-Myers
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引用次数: 7

Abstract

A case study is presented of a 5-year-old boy who was classified as preschool handicapped and was assessed as having a specific expressive language impairment with verbal apraxia. Chromosomal studies revealed a de novo (new) balanced translocation between first and second chromosomes. Results of the neurological, speech/language, cognitive, and play evaluations revealed a child with a severe expressive speech-language deficit but good nonverbal cognitive and communicative skills. The hypothesis of a relationship between a chromosomal translocation and speech/language disorders is explored.

患有特殊语言障碍和失用症儿童的染色体易位。
本文介绍了一个5岁男孩的个案研究,他被归类为学龄前残疾,并被评估为具有特定的表达性语言障碍和言语失用症。染色体研究揭示了第一和第二染色体之间的新平衡易位。神经学、言语/语言、认知和游戏评估的结果显示,该儿童具有严重的表达性言语语言缺陷,但具有良好的非言语认知和沟通能力。染色体易位和语言障碍之间的关系的假设被探索。
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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