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Apraxia of speech and cerebellar mutism syndrome: a case report

机译:言语和小脑突变突变综合征的症状:案例报告

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Cerebellar mutism syndrome (CMS) or posterior fossa syndrome (PFS) consists of a constellation of neuropsychiatric, neuropsychological and neurogenic speech and language deficits. It is most commonly observed in children after posterior fossa tumor surgery. The most prominent feature of CMS is mutism, which generally starts after a few days after the operation, has a limited duration and is typically followed by motor speech deficits. However, the core speech disorder subserving CMS is still unclear. This study investigates the speech and language symptoms following posterior fossa medulloblastoma surgery in a 12-year-old right-handed boy. An extensive battery of formal speech (DIAS?=?Diagnostic Instrument Apraxia of Speech) and language tests were administered during a follow-up of 6 weeks after surgery. Although the neurological and neuropsychological (affective, cognitive) symptoms of this patient are consistent with Schmahmann's syndrome, the speech and language symptoms were markedly different from what is typically described in the literature. In-depth analyses of speech production revealed features consistent with a diagnosis of apraxia of speech (AoS) while ataxic dysarthria was completely absent. In addition, language assessments showed genuine aphasic deficits as reflected by distorted language production and perception, wordfinding difficulties, grammatical disturbances and verbal fluency deficits. To the best of our knowledge this case might be the first example that clearly demonstrates that a higher level motor planning disorder (apraxia) may be the origin of disrupted speech in CMS. In addition, identification of non-motor linguistic disturbances during follow-up add to the view that the cerebellum not only plays a crucial role in the planning and execution of speech but also in linguistic processing. Whether the cerebellum has a direct or indirect role in motor speech planning needs to be further investigated.
机译:小脑突变综合征(CMS)或后肢体综合征(PFS)包括神经精神,神经心理学和神经源性语音和语言缺陷的星座。后窝肿瘤手术后的儿童最常观察到。 CMS最突出的特征是突变,其通常在操作后几天后开始,其持续时间有限,通常随后是电机语音缺陷。然而,核心语音障碍所储存的CMS仍然不清楚。本研究调查了一名12岁的右手男孩后浮肿髓质母细胞瘤手术后的语音和语言症状。在手术后6周后,在手术后6周内进行了大量的正式演讲(DIAS?=?诊断仪器的诊断仪器,语言测试)。虽然该患者的神经和神经心理学(情感,认知)症状与Schmahmann的综合征一致,但语音和语言症状明显不同于文献中通常描述的内容。关于语音生产的深入分析揭示了与诊断术语(AOS)的诊断一致的特征,而Axaxic Dysarthria完全没有。此外,语言评估显示出真正的失语缺陷,反映了语言的语言的产生和感知,WordFinding困难,语法干扰和口头流畅性缺陷。据我们所知,这种情况可能是第一个例子,清楚地表明,更高水平的电机规划障碍(APRAXIA)可能是CMS中断的讲话的起源。此外,在随访期间的非运动语言干扰的识别加入了小脑的观点,即小脑不仅在规划和执行中发挥着至关重要的作用,还在语言处理中发挥着至关重要的作用。大脑是否在电机语音规划中具有直接或间接作用,需要进一步调查。

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