Functional Localisation Flashcards

1
Q

area affected in CNS problem

A

hemiplegia

paraplegia

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2
Q

area affected in PNS

A

peripheral or localised area

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3
Q

area affected in NMJ

A

ocular
bulbar
proximal limb

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4
Q

area affected in muscle problem

A

proximal

symmetrical

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5
Q

description of weakness in CNS problem

A

heaviness

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6
Q

description of weakness in PNS problem

A

positional/with sleep

ascending

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7
Q

description of weakness in NMJ problem

A

fatiguable

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8
Q

description of weakness in muscle

A

aching

insidious

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9
Q

additional features in CNS problem

A

spasms

jerks

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10
Q

additional features in PNS problem

A

cramp

twitching

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11
Q

additional features in NMJ problem

A

bulbar= swallowing, speaking
ocular=diplopia, ptosis
respiratory= orthopnoea, SOB

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12
Q

additional features in muscle problem

A

myalgia

cramp

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13
Q

sensory symptoms in CNS problem?

A

yes

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14
Q

sensory symptoms in PNS problem?

A

yes

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15
Q

sensory symptoms in NMJ

A

no

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16
Q

sensory symptoms if muscle problem?

17
Q

tone in CNS problem

A

increased
spasticity
clonus

18
Q

tone in PNS problem

19
Q

pattern of weakness in CNS

A

pyramidal

arm extensors and leg flexors

20
Q

pattern of weakness in PNS problem

A

distal weakness

21
Q

reflexes in CNS problem

A

increased in CNS

22
Q

reflexes in PNS problem

23
Q

plantar response in CNS

24
Q

plantar response in PNS

25
weakness if lesion cervical spine?
weakness in arms and legs
26
weakness if lesion in thoracolumbar spine
weakness in legs
27
LMN causes
anterior horn of spinal cord symmetrical polyneuropathy mononeuropathy
28
what is symmetrical polyneuropathy a complication of?
diabetes toxins (alcohol) metabolic insults inheritable disorders
29
causes of mononeuropathy
``` nerve compression mononeuritis multiplex (diabetes or vasculitis) ```
30
classification of movement disorders
1. corticospinal/pyramidal 2. basal ganglia (extra-pyramidal) 3. cerebellum
31
corticospinal/pyramidal movement disorder presentation
pyramidal weakness and spasticity
32
basal ganglia movement disorder presentation
hyperkinetic | hypokinetic
33
cerebellum movement disorder presentation
wide-based gait tremor ataxia
34
function of the frontal lobe
``` executive functioning motivation hunger sexual function responsibilities ```
35
dysfunction of the frontal lobe signs
``` personality change magnetic gait (feet attached to the floor) seizures incontinence visual fields (optic chiasm) Broca's area anosmia ```
36
temporal lobe dysfunction signs
``` memory dysfunction agnosia Werncike's area visual fields auditory dysfunction limbic dysfunction temporal lobe epilepsy ```
37
parietal lobe dysfunction signs
``` visual field defect sensory dysfunction Gerstmann's syndrome dyspraxia change in handwriting inattention denial ```