ABCN deck 4 Flashcards

1
Q

For PSP, dementia occurs in __ to __% of cases.

A

50-80

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2
Q

impairment in the ability to control movements, characterized by spasmodic or repetitive motions or lack of coordination

A

dyskinesia

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3
Q

Movement disorder associated with atrophy of putamen, pons, middle cerebral peduncles, cerebellum, medulla oblongata, and dilation of 4th ventricle.

A

MSA

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4
Q

which CN? provides sensory innervation to the face, nasal sinuses, mouth, tongue; mastication

A

trigeminal, CN V

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5
Q

atrophy, fasciculations, and hyporeflexia can be indicative of ___ lesions.

A

LMN

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6
Q

EEG wave? observed in children during sleep. more prominent during drowsiness.

A

theta

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7
Q

hyperreflexia, increased tone, and pronator drift can be indicative of ___ lesions.

A

UMN

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8
Q

Core diagnostic symptoms of ___ include vertical gaze palsy, axial rigidity, and postural instability with falls (often backward).

A

PSP

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9
Q

What movement disorder is associated with insoluble 4-repeat tau protein deposits and dopamine depletion in the substantia nigra, caudate, and putamen; neuronal loss in the globus pallidus, subthalamic nuclei, red nuclei, dentate nucleus, superior colliculi, and periqueductal gray matter?

A

PSP

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10
Q

Onset of cortical basal syndrome usually occurs in the ___s but ranges from the __s to ___s.

A

60s, 50s. 70s.

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11
Q

which CN? vision

A

optic. CN II.

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12
Q

EEG wave? observed in all age groups but more common in adults. Relaxed with eyes closed.

A

alpha

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13
Q

which cranial nerve? smell

A

olfactory nerve, CN 1

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14
Q

EEG wave? observed in all age groups. alert, anxious, eyes open.

A

beta

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15
Q

The most common neurological complications for preterm infants are

A

periventricular hemorrhagic infarction and periventricular leukomalacia.

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16
Q

__-__% of babies born < 25 weeks gestation have moderate to severe cognitive impairment.

A

30-70%

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17
Q

Which PSP subtype? progressive gait disturbance with freezing gait, speech or writing, rigidity, dementia or eye movement abnormality during first 5 years, no tremor

A

progressive gait freezing

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18
Q

which CN controls facial expressions?

A

facial nerve, CN VII

19
Q

Which PSP subtype? nonfluent primary progressive aphasia, later development of gait/balance problems, rarer presentation

A

speech language

20
Q

Which movement disorder is associated with atrophy of the midbrain tegmentum (hummingbird sign), and cerebellar peduncles?

21
Q

__ to __% of babies born < 25 weeks gestation develop cerebral palsy

22
Q

Dementia is less likely in ___, though deficits can be seen in EF, attention, visuo-spatial abilities, and aspects of memory later in the disease.

23
Q

which CN? innervates tongue muscles.

A

hypoglossal nerve, CN XII

24
Q

Which movement disorder? progressive, asymmetric ridigity, dyspraxia, cortical sensory loss, alien limb syndrome, bradykinesia, unresponsive to levodopa, rarer presentation

A

corticobasal syndrome

25
For PSP the most common cause of death is ___ or ___.
respiratory arrest due to pneumonia, degeneration of brainstem respiratory centers.
26
In ___, early cognitive symptoms typically include impairment in language production, EF, and attention/concentration.
cortical basal syndrome
27
oculomotor dysfunction occurs __ to __ years after symptoms begin in PSP.
3 to 4
28
EEG wave? observed during sleep across age groups. dominant rhythm in infants.
delta
29
Presenting symptoms of ___ are most frequently postural instability and falls.
PSP
30
inaccurate range of movement during motion-based activities.
dysmetria
31
Onset of PSP is typically in the ___s, but can occur in the ___s.
60, 40
32
which CN? auditory and vestibular functions
vestibulocochlear, CN VIII
33
Common symptoms of ___ include dysarthria, dysphagia, bradykinesia, gait disorder, cognitive impairment, behavioral changes
PSP
34
Which CN? eye movements, pupillary constriction
oculomotor, CN III
35
which movement disorder is associated with early symptoms of genitourinary dysfunction, autonomic hypotension, and REM behavioral disorder that can progress rapidly to include balance, speech, and coordination problems.
Multisystem atrophy
36
70% of patients with ___ have orthostatic hypotension.
MSA
37
Disease that involves erosion of subcortical structures, subcortical-cortical connections, leading to a triad of motor, cognitive, and emotional/personality symptoms.
PSP
38
Which PSP subtype? deterioration of personality social compartment, behavior, and cognition years before PSP-RS symptoms.
frontal presentation
39
In ___, motor symptoms are typically symmetrical and generally do not respond to L-dopa.
MSA
40
Mean age of onset for MSA is ___ to ___.
55 to 60.
41
In __ apraxia typically begins in one limb and spreads to other limbs within 2 years. continued degree of asymmetry is common.
cortical basal syndrome
42
In ___ neuroimaging may reveal focal, asymmetric cortical atrophy in the frontal/parietal areas and similar asymmetric hypoperfusion/hypometabolism.
cortical basal syndrome.
43
Which movement disorder is associated with asymmetric motor symptoms involving limb rigidity or akinesia, limb dystonia, limb myoclonus, limb apraxia, cortical sensory loss, and/or alien limb phenomenon
cortical basal syndrome