Patterns of Neurological Dysfunction Flashcards

1
Q

Where do extrapyramidal signs come from?

A

basal ganglia

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2
Q

Where do pyramidal signs come from?

A

Corticospinal /

pyramidal tract

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3
Q

What are the two types of extrapyramidal sings?

A

hyperkinetic hypokinetic

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4
Q

Signs of hyperkinetic (extrapyramidal) movement disorders?

A
Dystonia,
Tics,
Myoclonus
Chorea
(Tremor)
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5
Q

What is the term for spasmodic jerky contraction of groups of muscles?

A

myoclonus

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6
Q

Signs of hypokinetic movement disorders?

A

rigidity, bradykinesia

Parkinsonism

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7
Q

Name a hypokinetic movement disorder.

A

Parkinson’s disease

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8
Q

What is ataxia and what part of the brain does it come from?

A

loss of full control of bodily movements

cerebellum

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9
Q

What is a pyramidal lesion the same as?

A

upper motor neuron lesion

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10
Q

In which, upper or motor neuron lesions, are there decreased or absent reflexes?

A

lower

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11
Q

Symptoms of muscle disease?

A

wasting (usually proximal), decreased tone, decreased or absent tendon reflexes

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12
Q

Symptoms of neuromuscular junction disease?

A

fatiguable weakness, normal or decreased tone, normal tendon reflexes. No sensory symptoms

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13
Q

Symptoms of functional weakness?

A

no wasting, normal tone, normal reflexes, erratic power, non-anatomical loss

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14
Q

What occurs with acute stroke syndromes, space occupying lesions, and spinal cord problems ?

A

UPPER motor neuron lesions

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15
Q

What type of lesion is suggested by a contralateral pyramidal weakness in face, arm, leg?

A

hemispheric upper motor neuron

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16
Q

What occurs with Parasagittal frontal lobe lesion?

A

paraparesis

17
Q

In a spinal cord upper motor neuron lesion, where does weakness occur?

A

pyramidal weakness below the level of the lesion
cervical: arms and legs
Thoracolumbar: legs

18
Q

What disease pattern occurs with motor neuron disease, spinal muscular atrophy, (lead poisoning, poliomyelitis,…)?

A

LOWER - anterior horn cells

19
Q

How does peripheral nerve involvement with lower motor neurons present?

A

Symmetrical (often length dependent) polyneuropathy with weakness and sensory symptoms: frequent complication of diabetes. Other aetiologies include a variety of toxic (alcohol) or metabolic insults as well as heritable disorders (often young onset and skeletal deformities)
Mononeuropathy as a result of nerve compression (carpal or tarsal tunnel syndrome, ulnar neuropathy, radial neuropathy) or mononeuritis multiplex (asymmetric polyneuropathy), which occurs in the context of diabetes or vasculitis

20
Q

What type of sensory loss does stocking (and later glove) imply?

A

dependent neuropathy

21
Q

What does sensory level loss imply?

A

spinal cord lesion

22
Q

Haemianaestheisa suggests what?

A

contralateral cerebral lesion, or with no other signs a non-organic disorder

23
Q

Disscociated sensory loss with lost spinothalamic (temperature / pain) but preserved dorsal column (vibration, light touch, proprioception) suggests what?

A

hemicord damage (anterior spinal artery syndrome, Brown-Sequard syndrome, syringomyelia)

24
Q

What is Dysdiadochokinesis?

A

clumsy, fast, alternating movements

25
Q

Intention tremor / ataxia is assessed by what in the arms?

A

finger nose test

26
Q

Intention tremor / ataxia is assessed by what in the legs?

A

knee heel testing

27
Q

Which part of the brain enables self-criticism and trying again?

A

frontal lobe

28
Q

Why may anosmia occur with frontal lobe dysfunction?

A

olfactory pathway is beneath frontal lobe

29
Q

What type of memory dysfunction is particularly common in temporal lobe dysfunction?

A

episodic memory loss

30
Q

What is the treatment protocol for Parkinson’s?

A

Symptomatic treatment with Levodopa replacement or dopamine agonist
Multidisciplinary team management including Speech and language, OT, PT, exercise
For selected patients deep brain stimulation (subthalamic nucleus, globus pallidus int)