Clinical Assessment of Neurological Disorders Flashcards

(44 cards)

1
Q

What are the functions of the frontal lobe?

A

Intellectual function, praxis, inhibition, bladder continence, saccadic eye movement, motor function, expression of language.

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2
Q

What symptoms may occur in frontal lobe dementia?

A

Disinhibited behavior, sweet tooth, reduced smell, bladder dysfunction, gait apraxia, progressive motor dysphasia.

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3
Q

Where are primary motor neurons located?

A

Layer 4 of the motor cortex (Brodmann area 4).

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4
Q

Where do most motor fibers cross in the brain?

A

At the medullary pyramids.

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5
Q

What tract do most crossing motor fibers enter after decussation?

A

Lateral corticospinal tract.

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6
Q

A lesion in the right motor cortex causes weakness on which side?

A

Left (contralateral) upper motor neuron weakness.

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7
Q

A spinal cord lesion on the right side affects which side of the body?

A

Right side below the lesion (ipsilateral UMN signs).

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8
Q

What are signs of a left MCA territory stroke?

A

Right UMN facial weakness, expressive dysphasia, right arm > leg weakness.

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9
Q

What is the visual deficit in a left occipital lobe stroke?

A

Right homonymous hemianopia.

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10
Q

What functions are attributed to the parietal lobe?

A

Sensory integration and receptive language.

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11
Q

What occurs with a dominant parietal lobe lesion?

A

Dyslexia, acalculia, poor left-right discrimination, finger agnosia.

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12
Q

What symptoms occur with temporal lobe seizures?

A

Déjà vu, jamais vu, hallucinations, panic, fear, tonic-clonic seizures.

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13
Q

What type of sensation does the spinothalamic tract carry?

A

Pain and temperature.

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14
Q

Where do spinothalamic fibers cross?

A

At the level of the spinal cord entry.

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15
Q

What sensations do posterior column pathways carry?

A

Joint position, deep pressure, and vibration.

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16
Q

Where do posterior column fibers cross?

A

In the medulla.

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17
Q

What cranial nerves originate in the midbrain?

A

3, 4

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18
Q

Which cranial nerves originate in the pons?

19
Q

Which cranial nerves originate in the medulla?

A

9, 10, 11, 12

20
Q

What is Weber syndrome?

A

Ipsilateral CN III palsy and contralateral hemiparesis.

21
Q

What is Wallenberg syndrome?

A

Lateral medullary infarct with ipsilateral ataxia, Horner’s, vertigo, and contralateral sensory loss.

22
Q

What are the three functional regions of the cerebellum?

A

Vermis (balance), paravermis (tone), cerebellar hemispheres (fine coordination).

23
Q

What are the features of cerebellar dysfunction (VANISH’D)?

A

Vertigo, ataxia, nystagmus, intention tremor, slurred speech, hypotonia, dysmetria.

24
Q

Do cerebellar lesions cause ipsilateral or contralateral signs?

25
What functions are associated with thalamic regions?
Movement, sensation, mood, vision, and hearing.
26
What can result from a ventroposterior thalamic infarct?
Severe sensory loss and pain syndromes.
27
What are the components of a neurological exam?
Cognition, cranial nerves, motor, sensory, coordination, gait, Romberg's.
28
What are three tools used for cognitive assessment?
MMSE, ACE-R, MOCA.
29
What signs occur with a complete CN III lesion?
Eye down and out, dilated pupil, partial ptosis.
30
What is Horner’s syndrome?
Ptosis, miosis, anhidrosis—loss of sympathetic supply.
31
What distinguishes UMN vs LMN facial weakness?
UMN: lower face only (contralateral); LMN: full face (ipsilateral).
32
What are the key signs of upper motor neuron lesion (UMNL)?
Spasticity, hyperreflexia, Babinski sign.
33
What are signs of lower motor neuron lesion (LMNL)?
Flaccidity, atrophy, fasciculations, reduced reflexes.
34
How is muscle power graded?
From 0 (no movement) to 5 (normal power).
35
What does an extensor plantar response indicate?
UMN lesion (Babinski sign).
36
What is clonus?
Repetitive, rhythmic muscle contractions after stretch—sign of UMN lesion.
37
What sensations are tested for spinothalamic tract function?
Pain and temperature.
38
What sensations are tested for posterior column function?
Vibration and joint position.
39
What type of sensory loss occurs in Brown-Séquard syndrome?
Ipsilateral posterior column and motor loss; contralateral spinothalamic loss.
40
What is syringomyelia?
Central cord lesion causing dissociative sensory loss and possibly UMN signs.
41
What is anterior spinal artery syndrome?
Bilateral motor and spinothalamic loss, with spared posterior columns.
42
What is a spastic gait?
Stiff, scissoring pattern, often due to bilateral UMNL.
43
What is a Parkinsonian gait?
Shuffled, slow steps, festinant in advanced cases.
44
What is a cerebellar gait?
Broad-based, unsteady.