We have used the technique of PET to chart the cortical areas activate
d by visual motion in the brain of a patient with a severe impairment
in the ability to recognize the motion of objects (akinetopsia), follo
wing bilateral lesions which have so far been presumed to include area
V5. High resolution MRI of her brain showed that the zone occupied by
area V5 had indeed been destroyed bilaterally. Positron emission tomo
graphy activation images, co-registered to the MRIs, showed three prin
cipal regions of the cortex activated by motion. These were located (i
) bilaterally in the precuneus of superior parietal cortex (area 7 of
Brodmann); (ii) bilaterally in the cuneus (a region considered to repr
esent upper V3); (iii) in the left lingual and fusiform gyri (possibly
lower V3 and adjacent areas). In contrast to normal subjects, there w
as no significant activation of area V1 or V2. The stimuli used for sc
anning were chosen by prior testing of the patient's visual capacities
. The control stimulus was a static random distribution of light squar
es on a dark background In the moving stimulus these squares moved coh
erently, the direction of motion changing periodically between the car
dinal directions (left, right, up and down). It tons activated by the
stimuli used during scanning. ascertained that the patient could corre
ctly identify these directions. We also found (i) that her occasional
errors were always in the direction opposite to the motion presented,
so that her identification of axis of motion (i,e. vertical or horizon
tal) was 100% correct; (iii) that when a few static squares were added
to the moving display her identification of direction fell to chance
but her identification of the axis of motion remained 100%; (iii) that
when a few squares moving opposite and orthogonal to the predominant
direction of motion were incorporated, her performance on both directi
on and axis fell to chance; (iv) that she was unable to identify motio
n in oblique directions between the horizontal or vertical axes, alway
s guessing one of the cardinal directions. In accounting for her resid
ual vision in terms of cortex which remains active, we hypothesize: (i
i) that the bilateral loss of V5 has affected direction sensitive mech
anisms at other sites in the cortex which are interconnected with V5 a
nd (ii) that in consequence her performance on our tests reflects the
properties of dynamic orientation selective mechanisms that were also
differentially activated by the stimuli used during scanning.