Cognitive functions Flashcards

1
Q

Normal digit span

A

7+/-2

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2
Q

Most helpful orientation test

A

Time

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3
Q

Inaccuracy considered normal in date orientation

A

2 days or less

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4
Q

Disorder where disorientation to name is seen

A

Psychogenic amnesia

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5
Q

Usual error made in similarities test

A

Answering that they are different, being unable to consider similarities

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6
Q

Issue with proverb meanings test

A

Culturally and eduationally dependent

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7
Q

Area of brain lesion where neglect is usually seen

A

Right hemisphere inferior parietal or prefrontal

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8
Q

Hippocampal hemisphere used for declarative verbal memories

A

Left

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9
Q

Hippocampal hemisphere for non-verbal memories

A

Right

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10
Q

Process of strengthening the connection between two neurons on repeated communication which is felt may be the neuronal basis of memory

A

Long term potentiation

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11
Q

Chemical process which mediated long term potentiation

A

NMDA mediated Ca2+ entry in glutamate neurons

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12
Q

Brain structure which connects Broca’s area to Wernicke’s area

A

Arcuate fasciculus

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13
Q

Type of aphasia which is fluent but with loss of comprehension

A

Wernicke’s aphasia

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14
Q

Type of aphasia which is non-fluent but with comprehension intact

A

Broca’s aphasia

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15
Q

Site of lesion causing impairment only for comprehension of spoken words

A

Superior temporal pole - bilateral or left sided

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16
Q

Site of lesion causing pure word blindness/alexia without agraphia - patient can speak, understand spoken language, and write, but not understand written language

A

Splenium of corpus callosum and L visual cortex (usually due to L PCA infarct)

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17
Q

Area of brain lesion which causes isolated limb apraxia

A

Corticobasal degeneration

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18
Q

Type of apraxia which involves the inability to make elements into a meaningful whole e.g. draw diagrams

A

Constructional apraxia

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19
Q

Area of brain lesion which causes a constructional apraxia

A

Right parietal lobe

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20
Q

Type of apraxia which involves an inability to carry out sequences of actions

A

Ideational/conceptual apraxia

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21
Q

Areas of brain lesions which cause ideational apraxia

A

Left parieto-occipital and parieto-temporal lesions

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22
Q

Type of apraxia which the inability to carry out goal directed movements

A

Ideomotor apraxia

23
Q

Area of brain lesions which cause ideomotor apraxia

A

Frontal and parietal

24
Q

Type of apraxia which involves the inability to coordinate and carry out facial movements

A

Buccofacial apraxia

25
Area of brain lesion which causes buccofacial apraxia
Left inferior frontal lobe and insula
26
Type of apraxia which involves loss of hand and finger dexterity
Limb-kinetic apraxia
27
Area of brain lesion causing limb-kinetic apraxia
Dominant primary motor cortex
28
Failure of object recognition despite normal visual perception
Visual object agnosia
29
Area of brain lesion causing visual object agnosia
Bilateral occipitotemporal
30
Inability to recognise familiar faces
Prosopagnosia
31
Area of brain lesion causing acquired prosopagnosia
Fusiform gyrus
32
Colour deficit where there is the loss of ability to discriminate colours
Achromatopsia
33
Area of brain lesion causing achromatopsia
Left occipitotemporal damage (L PCA infarction)
34
Colour deficit where there is loss of ability to retrieve knowledge about colours e.g. colour of a banana
Colour agnosia
35
Area of brain lesion causing colour agnosia
Left occipitotemporal damage
36
Colour deficit where there is inability to name colours
Colour anomia
37
Brain lesion causing colour anomia
Disconnection of the language structures in the temporal lobe from the visual cortex
38
Inability to read, write, and comprehend numbers
Acalculia
39
Inability to perform mathematical calculations
Anarithmetrica
40
Three features of Balint syndrome
Simultanagnosia Optic ataxia Oculomotor apraxia
41
Area of brain lesion causing Balint syndrome
Bilateral superior parieto-occipital
42
Four features of Gerstmann syndrome
Dysgraphia Dyscalculia Finger agnosia Right left disorientation
43
Area of brain lesion causing Gerstmann syndrome
Dominant angular and supramarginal gyri of the parietal lobe
44
Feature of Anton syndrome
Cortical blindness and denial of same
45
Area of brain lesion causing Anton syndrome
Bilateral occipital damage
46
Features of Marchiafava-Bignami disease
Sudden onset stupor and seizures | Occasionally chronic onset dementia and gait issues
47
Substance associated with Marchiafava-Bignami disease
Red wine excess
48
Area of brain lesion causing Marchiafava-Bignami disease
Symmetrical demyelination and necrosis of corpus callosum and adjacent anterior commissure
49
Automatic behaviours which are correct, but inappropriate to the situation e.g. using a toothbrush that is in sight in the middle of a doctor's appointment, or taking a cigarette out of someone else's mouth and using it
Utilization behaviour
50
Behaviour which imitates the examiner's behaviour
Imitation behaviour
51
Behaviour where an object is repeatedly rubbed, held or manipulated
Manual groping behaviour
52
Behaviour where there are bizarre hand movements the patient feels no control over
Alien hand sign
53
Behaviour where there is an overreliance on environmental stimuli to guide behaviour
Environmental dependency syndrome