5.6 Pattern recognition in neurology Flashcards

1
Q

pyramidal
UMN features
-pyramidal weakness
-spasticity

A

corticospinal / pyramidal tract

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2
Q

EPS

A

basal ganglia

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3
Q

ataxia

A

cerebellum

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4
Q

truly generalised weakness should include

A

bulbar motor function

otherwise, quadri/tetraparesis

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5
Q

UMN pattern weakness is—?

A

weak extensors in arm

weak flexors in leg

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6
Q

causes of UMN pattern of weakness

A

stroke
SOL
spinal cord problems

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7
Q

what kind of pattern will these cause?

  • motor neuron disease
  • spinal muscular atrophy
  • lead poisoning
  • polimyelitis
A

anterior horn cell - lower motor neurone lesion

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8
Q

organophosphate poisoning inhibits which enzyme?

A

acetylcholinesterase

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9
Q

causes of hemicord damage symptoms

  • lost spinothalamic (temperature, pain)
  • preserved dorsal colum (vibration, light touch, proprioception)
A

anterior spinal artery syndrome
brown sequard syndrome
syingomyelia

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10
Q

cerebellar signs

A
broad unstead gait
intention tremor/ataxia
dysdiadochokinesis - clumsy fast alternating movements
nystagmus
dysarthria
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11
Q

damage here causes disinhibition

-hunger, thirst, sexual functions becomes disinhibited

A

orbitofrontal cortex

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12
Q

damage here causes decreased response to external stimuli

A

dorsolateral prefrontal cortex

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13
Q

damage here causes abulia - lack of will or akinetic mutism

A

cingulate gyrus and dorsomedial frontal lobe

-motivation is affected

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14
Q

where does auditory dysfunction localise to?

A

herschel’s gyrus of temporal lobe

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15
Q

syndrome:
- dysgraphia
- left right disorientation
- finger agnosia
- acalculia

A

Gerstmann’s syndrome

-disease of the domiant angual gyrus, in the inferior parital lobe

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16
Q

site of lesion for:

-inattention

A

non-dominant angular gyrus of parietal lobe

17
Q

where would deep brain stimulation work for parkinsons disease?

A

subthalamic nucleus

globus pallidus internal

18
Q

cross the blood brain barrier and act directly as D2-type receptors. These agents include pramipexole, ropinirole, and bromocriptine.

A

Dopamine agonists

19
Q

such as selegiline and rasagiline can improve symptoms in patients with mild disease (as monotherapy) as well patients already on levodopa.

A

MAO-B inhibitors

20
Q

such as trihexyphenidyl or diphenhydramine (Benadryl) aim to combat tremor, but usually cause severe side effects

A

Anticholinergics

21
Q

blocks NMDA receptors and has a mild attenuation of resting tremor and dystonia. May alleviate levodopa induced dyskinesias.

A

Amantadine

22
Q

diagnosis of MS

A

neurological assessment

MRI imaging brain- including gadolinium contrast

23
Q

primary lateral sclerosis- affects which modality

A

upper motor neurone ONLY

24
Q

what imaging identifies old lesions and lesions of non-vascular origin in ischaemic stroke?

A

MRI T1/2 and FLAIR imaging

25
Q

what imaging identifies new ischaemic lesions in stroke?

A

Diffusion weighted images
-hyperintensities in stroke
decreased signal on apparent diffusion coefficient of water

26
Q

What imaging for bleeds and microbleeds (stroke)?

A

T2

27
Q

What imaging for identifying brain areas at risk of ischaemia?

A

perfusion weighted images

28
Q

name the lesion
No visual field defect
No new higher cortical or brainstem dysfunction
Pure motor hemiparesis, or pure sensory deficit of one side of the body, or sensorimotor hemiparesis or ataxic hemiparesis (dysarthric clumsy hand syndrome or ipsilateral ataxia with crural hemiparesis)
At least 2 of the 3 areas (face, arm, leg) should be involved in its entity

A

lacunar syndrome

29
Q
name the syndrome- any 1 of: 
Cranial nerve palsy
Unilateral or bilateral motor or sensory deficit
Disorder of conjugate eye movements
Cerebellar dysfunction
Homonymous hemianopia
Cortical blindness
A

posterior circulation syndrome

30
Q

name the syndrome :
Hemiplegia and homonymous hemianopia contralateral to the lesion, and
Either aphasia or visuospatial disturbances
+/- sensory deficit contralateral to the lesion

A

total anterior circulation syndrome

31
Q

name the syndrome:
One or more of unilateral motor or sensory deficit, aphasia or visuospatial neglect (with or without homonymous hemianopia)
Motor or sensory deficit may be less extensive than in lacunar syndromes

A

partial anterior circulation syndrome