Oculomotor Impairments in Developmental Dyspraxia
Author(s) -
Bertrand Gaymard,
Marianna Giannitelli,
G. Challes,
Sophie Rivaud-Péchoux,
Olivier Bonnot,
David Cohen,
Jean Xavier
Publication year - 2016
Publication title -
the cerebellum
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.418
H-Index - 72
eISSN - 1473-4230
pISSN - 1473-4222
DOI - 10.1007/s12311-016-0817-6
Subject(s) - saccade , psychology , neuroscience , cerebellum , alertness , eye movement , cognition , neurophysiology , audiology , medicine , psychiatry
Children with developmental dyspraxia (DD) express impairments in the acquisition of various motor skills and in the development of their social cognition abilities. Although the neural bases of this condition are not fully understood, they are thought to involve frontal cortical areas, subcortical structures, and the cerebellum. Although cerebellar dysfunction is typically difficult to assess and quantify using traditional neurophysiological methods, oculomotor analysis may provide insight into specific cerebellar patterns. The aim of the present study was to investigate, in dyspraxic and typically developing subjects, various oculomotor saccade tasks specifically designed to reveal frontal and cerebellar dysfunction. In addition to evidence supporting prefrontal dysfunction, our results revealed increased variability of saccade accuracy consistent with cerebellar impairments. Furthermore, we found that dyspraxic patients showed decreased velocities of non-visually guided saccades. A closer analysis revealed significant differences in saccade velocity profiles with slightly decreased maximum saccade velocities but markedly prolonged deceleration phases. We show that this pattern was not related to a decreased state of alertness but was suggestive of cerebellar dysfunction. However, the clear predominance of this pattern in non-visually guided saccades warrants alternative hypotheses. In light of previous experimental and anatomical studies, we propose that this unusual pattern may be a consequence of impaired connections between frontal areas and cerebellar oculomotor structures.
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