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Abstract:
The role of fronto-striatal circuits in visuomotor learning
is still highly debated (Wise, 1996). Some have suggested that
populations with fronto-striatal dysfunctions may show difficulties
with visuomotor acquisition of mirror-inverted movements. We have
recently shown that patients with frontal lesions are impaired in
the first trials of mirror-inverted movements (Richer et al.,
1999). This study aimed at comparing the performance of patients
with frontal excisions, early Huntingtons disease and Tourette
syndrome to matched control groups, on mirror-inverted reaching
movements on a graphics tablet. In non-inverted reaching movements,
all groups showed normal precision measured by trajectory length.
When feedback was mirror-inverted, controls produced movements
containing large trajectory corrections in the first trials and
improved dramatically after 32 trials. Frontal patients showed poor
corrections in the first phase of adaptation but reached normal
level after 32 practice trials, indicating problems with the
attentional control of novel movements. Tourette patients showed
normal trajectories in the first phase of adaptation but their
precision did not further improve after 20 trials, suggesting
normal control of novel movements but difficulties in late
acquisition. HD patients showed problems before and after practice,
suggesting that they combine problems of frontal and Tourette
patients. These results indicate a dissociation between the
visuomotor processes affected in these populations. This
dissociation suggests that different components of fronto-striatal
circuitry may be involved in different phases of visuomotor
learning.
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