Processamento auditivo, leitura e escrita na síndrome de Silver-Russell: relato de caso

Patrícia Fernandes Garcia, Karina Krähembühl Salvador, Tâmyne Ferreira Duarte de Moraes, M. R. Feniman, Patrícia Abreu Pinheiro Crenitte
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引用次数: 2

Abstract

The aim of this study was to describe the speech-language pathology aspects of auditory processing, reading and writing of a male patient diagnosed with Silver-Russell syndrome. With two months of age the patient presented weight-for-height deficit; broad forehead; small, prominent and low-set ears; high palate; discrete micrognathia; blue sclera; cafe-au-lait spots; overlapping of the first and second right toes; gastroesophageal reflux; high-pitched voice and cry; mild neuropsychomotor development delay; and difficulty to gain weight, receiving the diagnosis of the syndrome. In the psychological evaluation, conducted when he was 8 years old, the patient presented normal intellectual level, with cognitive difficulties involving sustained attention, concentration, immediate verbal memory, and emotional and behavioral processes. For an assessment of reading and writing and their underlying processes, carried out at age 9, the following tests were used: Reading Comprehension of Expository Texts, Phonological Abilities Profile, Auditory Discrimination Test, spontaneous writing, Scholastic Performance Test (SPT), Rapid Automatized Naming Test (RANT), and phonological working memory. He showed difficulties in all tests, with scores below expected for his age. In the auditory processing assessment, monotic, diotic and dichotic tests were conducted. Altered results were found for sustained and selective auditory attention abilities, sequencial memory for verbal and non-verbal sounds, and temporal resolution. It can be concluded that the patient presents alterations in the learning of reading and writing that might be secondary to the Silver-Russell syndrome, however, these difficulties can also be due to deficits in auditory processing abilities.
Silver-Russell综合征的听觉加工、阅读和写作1例
本研究的目的是描述一个被诊断为西尔弗-罗素综合症的男性患者的听觉处理、阅读和写作的语言病理学方面。两个月大时,患者出现体重身高比不足;宽阔的额头上;小的,突出的和低的耳朵;高口感;离散小颌畸形;蓝色巩膜;浅褐色斑点;右脚趾头和右脚趾头重叠的;胃食管反流;高亢的声音和哭声;轻度神经精神运动发育迟缓;而且体重难以增加,被诊断为该综合征。在8岁时进行的心理评估中,患者智力水平正常,但存在持续注意力、注意力集中、即时言语记忆、情绪和行为过程方面的认知困难。为了评估9岁儿童的阅读和写作及其基本过程,使用了以下测试:说明性文本阅读理解、语音能力特征、听觉辨别测试、自发写作、学业表现测试(SPT)、快速自动命名测试(RANT)和语音工作记忆。他在所有考试中都表现出困难,分数低于他这个年龄的预期。在听觉加工评定中,采用单、二、二分测验。结果发现,持续和选择性听觉注意能力、语言和非语言声音的顺序记忆以及时间分辨率发生了变化。可以得出结论,患者在阅读和写作学习方面的改变可能是继发于西尔弗-罗素综合征,然而,这些困难也可能是由于听觉处理能力的缺陷。
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