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一名患有右侧额颞叶变性患者对人物及其他独特实体的跨模态识别障碍

Cross-modal recognition disorders for persons and other unique entities in a patient with right fronto-temporal degeneration.

作者信息

Gainotti Guido, Ferraccioli Monica, Quaranta Davide, Marra Camillo

机构信息

Neuropsychology Service of the Policlinico Gemelli, Catholic University of Rome, Italy.

出版信息

Cortex. 2008 Mar;44(3):238-48. doi: 10.1016/j.cortex.2006.09.001. Epub 2007 Nov 17.

Abstract

We describe a patient (CD), with a right fronto-temporal degeneration, who showed massive defects in the recognition of familiar people and severe behavioural disorders. CD scored in the normal range on tests of episodic memory, attention and visual-spatial abilities, and obtained mildly abnormal scores on naming and executive functions tests. CD was then studied and matched with a left brain-damaged patient (IG), comparable to her as for education, naming score and general cognitive impairment, on several tasks, exploring recognition of familiar people and of other instances of 'unique entities'. On specific tasks of face recognition, she obtained normal results on perceptual tests, but highly pathological scores on mnesic-associative tasks. A similar defect was found when identification was based on the person's voice or on a verbal definition. The cross-modal nature of CD's disorder was confirmed by results of a test, in which person-specific information available from photographs and from names was directly compared. In order to evaluate if CD's recognition disorder: (a) was the consequence of a general semantic defect, (b) was specific for people, or (c) also concerned other instances of 'unique entities', we matched her capacity to name and recognize the pictures of items belonging to various categories of knowledge with those concerning famous monuments and famous people. CD identified items belonging to semantic categories much better than those considered as 'unique entities' and, within the latter, obtained slightly better results with famous monuments than with famous persons. MRI showed a bilateral atrophy of the antero-inferior parts of the temporal lobes, more pronounced in the right side. About 2 years after the onset of the symptomatology, CD became untestable, due to the development of a severe motor neuron disease.

摘要

我们描述了一位患有右侧额颞叶变性的患者(CD),她在识别熟悉的人方面存在大量缺陷,并伴有严重的行为障碍。CD在情景记忆、注意力和视觉空间能力测试中得分处于正常范围,在命名和执行功能测试中得分略有异常。随后,对CD进行了研究,并与一名左脑损伤患者(IG)进行匹配,IG在教育程度、命名得分和一般认知障碍方面与她相当,对他们进行了多项任务测试,以探究对熟悉的人和其他“独特实体”实例的识别情况。在人脸识别的特定任务中,她在感知测试中得到正常结果,但在记忆联想任务中得分极高,呈病态。当基于人的声音或言语定义进行识别时,也发现了类似的缺陷。一项测试结果证实了CD障碍的跨模态性质,该测试直接比较了从照片和名字中获取的特定人物信息。为了评估CD的识别障碍:(a)是否是一般语义缺陷的结果,(b)是否特定于人,或(c)是否也涉及其他“独特实体”实例,我们将她命名和识别属于各类知识范畴物品图片的能力,与识别著名纪念碑和名人图片的能力进行了匹配。CD识别属于语义范畴的物品比识别被视为“独特实体”的物品要好得多,在后者中,识别著名纪念碑的结果比识别名人的结果略好。磁共振成像显示颞叶前下部双侧萎缩,右侧更为明显。在症状出现约两年后,由于严重运动神经元疾病的发展,无法再对CD进行测试。

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