Abstract

Partial or complete Balint's syndrome is a core feature of the clinico-radiological syndrome of posterior cortical atrophy (PCA), in which individuals experience a progressive deterioration of cortical vision. Although multi-object arrays are frequently used to detect simultanagnosia in the clinical assessment and diagnosis of PCA, to date there have been no group studies of scene perception in patients with the syndrome. The current study involved three linked experiments conducted in PCA patients and healthy controls. Experiment 1 evaluated the accuracy and latency of complex scene perception relative to individual faces and objects (color and grayscale) using a categorization paradigm. PCA patients were both less accurate (faces < scenes < objects) and slower (scenes < objects < faces) than controls on all categories, with performance strongly associated with their level of basic visual processing impairment; patients also showed a small advantage for color over grayscale stimuli. Experiment 2 involved free description of real world scenes. PCA patients generated fewer features and more misperceptions than controls, though perceptual errors were always consistent with the patient's global understanding of the scene (whether correct or not). Experiment 3 used eye tracking measures to compare patient and control eye movements over initial and subsequent fixations of scenes. Patients' fixation patterns were significantly different to those of young and age-matched controls, with comparable group differences for both initial and subsequent fixations. Overall, these findings describe the variability in everyday scene perception exhibited by individuals with PCA, and indicate the importance of exposure duration in the perception of complex scenes.

Highlights

  • IntroductionBalint’s syndrome (simultanagnosia, optic ataxia, and ocular apraxia) is a central feature of the clinico-radiological syndrome of posterior cortical atrophy (PCA; Benson et al, 1988)

  • Balint’s syndrome is a central feature of the clinico-radiological syndrome of posterior cortical atrophy (PCA; Benson et al, 1988)

  • In the current study we examine the ability of individuals with PCA to categorise scenes relative to single items such as objects and faces (Experiment 1) and to describe what they perceive when viewing a photograph of a real world scene (Experiment 2)

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Summary

Introduction

Balint’s syndrome (simultanagnosia, optic ataxia, and ocular apraxia) is a central feature of the clinico-radiological syndrome of posterior cortical atrophy (PCA; Benson et al, 1988). Degeneration have been reported (e.g., Renner et al, 2004). In addition to partial or complete Balint’s syndrome, prominent cognitive impairments include visuoperceptual and other visuospatial impairments, alexia, Gerstmann’s syndrome (acalculia, agraphia, finger agnosia, left–right disorientation), and limb apraxia (O’Dowd and de Zubicaray, 2003; Tang-Wai et al, 2004; McMonagle et al, 2006; Lehmann et al, 2011a). Many of the visual deficits commonly reported in PCA are underpinned by basic visual deficits of elementary form and motion processing (Lehmann et al, 2011a).

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