Psychoanatomical substrates of Balint's syndrome

Психоанатомические субстраты синдрома Балинта
Manfredi Rizzo
2002-02-01

Balint's syndromeocular apraxiaoptic ataxiasimultanagnosiavisual attention
OBJECTIVES: From a series of glimpses, we perceive a seamless and richly detailed visual world. Cerebral damage, however, can destroy this illusion. In the case of Bálint's syndrome, the visual world is perceived erratically, as a series of single objects. The goal of this review is to explore a range of psychological and anatomical explanations for this striking visual disorder and to propose new directions for interpreting the findings in Bálint's syndrome and related cerebral disorders of visual processing. METHODS: Bálint's syndrome is reviewed in the light of current concepts and methodologies of vision research. RESULTS: The syndrome affects visual perception (causing simultanagnosia/visual disorientation) and visual control of eye and hand movement (causing ocular apraxia and optic ataxia). Although it has been generally construed as a biparietal syndrome causing an inability to see more than one object at a time, other lesions and mechanisms are also possible. Key syndrome components are dissociable and comprise a range of disturbances that overlap the hemineglect syndrome. Inouye's observations in similar cases, beginning in 1900, antedated Bálint's initial report. Because Bálint's syndrome is not common and is difficult to assess with standard clinical tools, the literature is dominated by case reports and confounded by case selection bias, non-uniform application of operational definitions, inadequate study of basic vision, poor lesion localisation, and failure to distinguish between deficits in the acute and chronic phases of recovery. CONCLUSIONS: Studies of Bálint's syndrome have provided unique evidence on neural substrates for attention, perception, and visuomotor control. Future studies should address possible underlying psychoanatomical mechanisms at "bottom up" and "top down" levels, and should specifically consider visual working memory and attention (including object based attention) as well as systems for identification of object structure and depth from binocular stereopsis, kinetic depth, motion parallax, eye movement signals, and other cues.
1
Although traditionally attributed to bilateral parietal lesions, Bálint’s syndrome can arise through other lesions and mechanisms, with dissociable components overlapping hemineglect.
2
Bálint’s syndrome disrupts coherent visual perception, producing simultanagnosia and visual disorientation in which scenes are experienced as isolated objects.
3
Existing evidence is heavily based on biased case reports, inconsistent definitions, inadequate basic-vision assessment, poor lesion localization, and insufficient separation of acute versus chronic deficits.
4
Future research should investigate bottom-up and top-down mechanisms involving visual working memory, attention—including object-based attention—and object-structure identification.
5
The syndrome also impairs visuomotor control, causing ocular apraxia and optic ataxia affecting eye and hand movements.

Bálint's syndrome and its associated cerebral visual-processing disorders

The psychological and anatomical mechanisms underlying disturbances of visual perception and visuomotor control, including simultanagnosia, visual disorientation, ocular apraxia, and optic ataxia

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2002-02-01
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Manfredi Rizzo
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