11) Perception, Agnosia, etc. Flashcards

1
Q

What is agnosia?

A

= visual information is transported via retina but cannot be processed –> objects (and faces) cannot be recognised

  • apperceptive agnosia = failure in perception and therefore recognition
  • associative agnosia = perception occurs but still not recognised –> V1 ok but association between visual and semantic brain areas defect
  • lesions often occur due to hypoxia or reanimation
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2
Q

What are the principles of retinotopy?

A
  • things are represented next to each other in the brain and visual field
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3
Q

What are the three retinal ganglia cells?

A

M-cells - magnolayer
- 10% of ganglia cells
- large receptive fields
- small spatial but good temporal resolution
- high contrast sensitivity
- achromatic (colour blind)

P-cells - parvolayer
- 80% of ganglia cells
- small receptive fields
- high spatial but poor temporal resolution
- small contrast sensitivity
- chromatic (colour competent)

Gamma-cells
- 10% of retinal ganglia cells
- heterogeous properties

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4
Q

Why are retinal ganglia cells well myelinated?

A

good for motion processing, because faster signal transmission

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5
Q

How is the lateral geniculate nucelus (LGN) organised and what does it do?

A

organised in layers
- magnolayers
- parvolayers
- interlaminar layers

  • forwards information to primary visual cortex/V1/striate cortex/BA17 (= only area in the brain where one can see stripes just when slicing the brain, no additional staining needed)
    –> visual information is from V1 forwarded to other areas in visual cortex (BA16-19/V1-V4) (?)
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6
Q

What are the retino-genikulo-striate pathways?

A

N Suprachiasmaticus
- circadian rhythm
- dark-light perception

Colliculus superior
- rapid eye movement
–> colliculus inferior: auditory

Corpus geniculate laterale
(- still unclear what it does, but postulated to be involved in spatial processing of objects in visual field and temporal differentiation of the same object at different time points)

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7
Q

How does the (primary) visual cortex process information (Hubel&Wiese)?

A

Ice-cube model
- organised in columns
- cells in column only react to a certain characteristic in the visual field (orientation, intensity..)
–> extraction of characteristics

(- same principle ‘Eigenschaftsextraktion’/extraction of characteristics found auditory cortex but more bitalerally)

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8
Q

Hemifield and hemispheres: how is it represented?

A

hemifield
Right hemifield:
- visual information of the temporal part of the retina of the right eye
- information of the nasal of the retina of the left eye

Left hemifield :
- temporal part of rentina (left eye)
- nasal part of the retina (right eye)

Viusal field
= the total area in which objects can be seen in the side (peripheral) vision as you focus your eyes on a central point

Hemispheres
- left and right side of the brain

  • information of the right hemifield is represented in the left hemisphere
  • information of the left hemifield is represented in the right hemisphere
  • information is represented mirrored (left-right and up-down’
  • everything in the centre is more polar (over representation of fovea)
  • periphery more to the front
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9
Q

Hierarchy in the visual cortex

A

from V1 to V5
- V1 most accurate in retinotopy - V4 and V5 least accurate in retinotopy
- V1 least complex (specific to responses, 1° resolution) - V4 and V5 most complex (specialised, 20° resolution)

  1. V1
    - most accurate in retinotopy but less complex information processing
    - contrast and orientation
  2. V2
    - differentiation background and figures
  3. V3a
    - disparity/incongruity/discrepancy –> mismatch when looking at a face from different angles
    - depth
  4. V4
    - colour and form
    - ventral: closer to temporal cortex (memory), remembering faces, objects etc –> recognition
  5. V5
    - motion, movement
    - dorsal: closer to motor areas, motion/movement via dorsal stream –> system advantage (vision guided movements)
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10
Q

What are the dorsal and ventral stream?

A

dorsal stream
= where/ how/ action/ location/ egocentric
- closer to motor areas, V5

ventral stream
= what/ object/ perception/ allocentric
- closer to temporal cortex, V4

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11
Q

Network map and complexity

A
  • more complex than described (dorsal vs ventral)

–> complex motion perception involves more

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12
Q

Retinotopy and lesions: What does it mean for patients?

A

lesions at different points in the system cause different visual impariments

contralateral homonymous hemianopia: lesion after optic chiasm (D), in optic radiations (G) or in upper and lower bank of the calcarine fissure (H)

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13
Q

What is homoymous hemianopia?

A

= lesion in occipital cortex (upper and lower banks of calcarine fissure), lesion after optic chiasm or optic radiations (one-side)
- both eyes –> always temporal (one eye) and nasal (the other eye) fibers

  • often people are nor aware they had a stroke because they don’t see ‘a black field’ –> aren’t aware that something is missing
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14
Q

What is achromatopsia?

A

= a higher dysfunction (not in the retina), caused by a stroke/lesion
–> NOT genetic (genetic = retina)

  • gyrus lingualis and gyrus fusiformus
    –> 9% of cerebral visual disorders
  • depending on where the lesion is, it can effect the upper visual field or is related to other agnosias
  • patients complain that things look dirty/sad
    -nothing much can be done to get colour vision back
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15
Q

Neuronal implementation (retinotopy) of object and face perception

A
  • less precise retinotopy but more complex (specialised)
  • contralateral and ipsilateral
  • 25-30° receptive field size
  • functional specialisation: complex
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16
Q

Alexia without agraphia?

A

= visuoverbal disconnection

  • hemanopia to the right
  • later quadrant anopsie
  • difficulties in spatial orientation, initially disturbed colour vision
  • additional lesion: information is not sent to corpus callosum –> not able to read
    –> BUT rest intact: can write
  • some regeneration possible: patients can learn to read again
  • hypertension, nikotin, diabetes, adipositas
17
Q

What is prosopagnosia?

A

= face blindness, faces cannot be recognised properly (only highly contrasted and stylised faces can be recognised)

  • temporal side: gyrus fusiformus and gyrus lingualis
  • large latency to discover something is wrong
  • if stylised like a face –> recognised as one (object and face recognition impaired)
18
Q

What is akinetopsia?

A

= motion blindness, motion is not perceived in a fluent wys but as stagnant pictures

  • bilateral lesion in medial temporal gyrus –> V5 rarely affected
  • gyrus temporalis medialis
  • often combined with lower quadrant field defects, optic ataxia and neglect
  • no fluent processing, objects jump by frame, no continuity of rising liquids

MT = retinotopic representation of visual motion
dMST = object motion
IMST: retinal slip by self or eye motion

  • good remission
19
Q

What is neglect?

A

= most common disorder of parietal lesion, lack of attention (in one hemisphere) to sensory stimuli or motor function, syndrome of contralaterl suppression of sensory stimuli

  • mostly right hemisphere in inferior parietal lobe
  • often combined with: hemianopia, neglect in further modality, anosognosia (=being cognitively unaware of disability)
20
Q

Test for neglect?

A
  1. copying
    - patient needs to copy picture –> usually only draw half of it
  2. Poppelreuther Durchstreichtest
    - patient needs to cross all horizontal lines –> usually only cross out half of the lines
  3. Line bisection test
    - patient needs to draw a vertical line to part lines in the middle (lines are of different length and skewed to one side) –> usually cannot mark the middle
  • hemianopia patients usually overcompensate
  • difficult to compensate for neglect patients but with awareness and practice can become better
21
Q

Pathophysiology of negelct

A

Usually after right parietal lesions
- but also possible after:
–> lesions in cingulum
–> lesions in PFC
–> lesions in thalamus
–> lesions in striatum

Reason
- disruption of the reticulo-thalamo-cortico-limbic loop

21
Q

Course of neglect

A
  • sponatenous restitution in 75% within 6 months
  • extend correlates with size and location but not with gender or age
  • affects other neurological functions