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先天性面孔失认症中的视觉心理意象

Visual mental imagery in congenital prosopagnosia.

作者信息

Grüter Thomas, Grüter Martina, Bell Vaughan, Carbon Claus-Christian

机构信息

University of Bamberg, Faculty of Humanities, Department of General Psychology and Methodology, 96047 Bamberg, Germany.

出版信息

Neurosci Lett. 2009 Apr 10;453(3):135-40. doi: 10.1016/j.neulet.2009.02.021. Epub 2009 Feb 14.

Abstract

Congenital prosopagnosia (cPA) is a selective impairment in the visual learning and recognition of faces without detectable brain damage or malformation. There is evidence that it can be inherited in an autosomal dominant mode of inheritance. We assessed the capacity for visual mental imagery in 53 people with cPA using an adapted Marks' VVIQ (Vividness of Visual Imaging Questionnaire). The mean score of the prosopagnosic group showed the lowest mental imagery scores ever published for a non-brain damaged group. In a subsample of 12 people with cPA, we demonstrated that the cPA is a deficit of configural face processing. We suggest that the 'VVIQ-PA' (VVIQ-Prosopagnosia) questionnaire can help to confirm the diagnosis of cPA. Poor mental imagery, a configural face processing impairment and clinical prosopagnosia should be considered as symptoms of a yet poorly understood hereditary cerebral dysfunction.

摘要

先天性面孔失认症(cPA)是一种在无明显脑损伤或畸形的情况下,对面孔进行视觉学习和识别的选择性障碍。有证据表明,它可以以常染色体显性遗传模式遗传。我们使用经过改编的马克斯视觉意象生动性问卷(VVIQ)评估了53名患有cPA的人的视觉心理意象能力。面孔失认症组的平均得分显示出非脑损伤组所公布的最低心理意象分数。在12名患有cPA的人的子样本中,我们证明cPA是一种对面孔结构加工的缺陷。我们建议“VVIQ-PA”(VVIQ-面孔失认症)问卷有助于确诊cPA。心理意象差、面孔结构加工受损和临床面孔失认症应被视为一种尚未被充分理解的遗传性脑功能障碍的症状。

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