Correlative Neuro Exam Flashcards

1
Q

Mental status options

A

alert, lethargic, stuporous, obtunded, comatose

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2
Q

decreased alertness: cause?

A

dysfunction of b/l cerebral hemispheres or brainstem reticular activating system

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3
Q

types of involuntary movements

A

tremor (resting or essential), myoclonus, chorea, athetosis (slow, writhing mvmt), ballismus, tics, seizures, dystonia (sustained abnormal posture), tardive dyskinesia, akathisia (motor restlessness)

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4
Q

asterixis

A
  • have pt stop traffic w/ wrists extended; beats of flexion = asterixis
  • possibly caused by metabolic encephalopathy ex: UTI, urosepsis, etc.
  • a negative myoclonus; cessation of m. activity
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5
Q

possible abnormal speech findings

A

dysphonia, dysarthria (impaired motor function needed for speech - not a language disorder), fluency, comprehension, repetition, aphasia

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6
Q

broca’s aphasia

A

nonfluent, comprehension spared, impaired repetition

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7
Q

Wernicke’s aphasia

A

fluent, impaired comprehension and repetition

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8
Q

global aphasia

A

deficits in all language functions

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9
Q

conductive aphasia

A

frequent paraphasic errors (usually phonemic), impaired repetition
phonemic error = substituting a similar word for a sound i.e. saying pish instead of fish

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10
Q

transcortical motor aphasia

A

repetition intact, pt can comprehend but is not fluent

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11
Q

transcortical sensory aphasia

A

pt is fluent and can repeat but impaired comprhension

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12
Q

transcortical mixed aphasia

A

pt can only repeat; no fluency or compehension

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13
Q

anomic aphasia

A

memory deficits; pt can’t name the word for a particular item

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14
Q

CNI: injury w/ likely cause

A

injury = anosmia
u/l causes = trauma or tumor
b/l causes = virus, allergy, smoking, trauma
head/face trauma, nose surgery, infections, obstructions, lesions at base of frontal lobe, aging
central anosmia can be caused by alcoholism, Alzheimer’s or parkinson’s

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15
Q

Foster Kennedy Syndrome

A

S&S: anosmia, i/l optic atrophy, c/l papilledema
associated w/ lesions of anterior skull base or frontal lobe
ex: meningioma arising from olfactory groove

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16
Q

anisocuria

A
  • unequal pupils
  • sympathetic nervous system and CNIII
  • hippus = normal brief oscillations of pupil size in response to light
  • if pupils more unequal in dark the small one is the problem eye; if there is more unevenness in the light the dilated one is the problem
17
Q

Marcus-Gunn pupil aka APD

A

afferent pupil defect = APD
can be seen w/ interruption of optic pathway anterior to optic chiasm
dx via the swinging flashlight test
seen w/ optic n. or retinal disease

18
Q

Adie pupil

A
  • can be u/l or b/l dilated pupil
  • lesion is in the ciliary ganglion
  • parasympathetic denervation: pupils react poorly to light but ok w/ accommodation; pupils redilate slowly
  • common manifestation of Holmes Adie Syndrome = benighn often familial disorder affecting young women
  • can be associated w/ depressed DTRs, segmental anhidrosis, orthostatic hypotension, cardiovascular autonomic instability
19
Q

Argyll Robertson Pupil

A
  • aka prostitute’s eye = accommodation but no reaction
  • small, irregular pupils
  • lesion involves descending pupilloconstrictor fibers
  • cause = neurosyphilis; could also be from lesions in EWN (ex: MS)
20
Q

CNIII, IV, VI problems

A
  • diplopia
  • ptosis = lesion in sympathetics, CNIII, NMJ, or from a m. disorder
  • pseudoptosis = redundant skin folds associated w/ aging
21
Q

nystagmus

A
  • involuntary, rapid, rhythmic mvmts of eye = oscillopsia
  • named for direction of quick component
  • if pathologic causes = meds, peripheral vestibular apparatus, central vestibular pathways, cerebellum
  • up to 50% of people have a small degree of nystagmus in extreme gaze
22
Q

Ptosis

A
  • CNIII dysfunction
  • eye appears “down and out”
  • pupil can be spared or impaired
23
Q

vertical diplopia

A
  • pt may have hypertropia: visual axis of one eye is higher than the other
  • head tilt to opposite side improves vision
  • could be caused by head trauma; CNIV dysfunction
24
Q

horizontal diplopia

A
  • CNVI dysfunction possibly caused by high ICP
  • could have esotropia = eye on one side looks turned in
  • head tilt to the same side improves vision
25
face droop
LMN: weakness or paralysis of 1/2 of the face; can be from peripheral n. or brainstem (pons) injury UMN: weakness of lower quarter of face; lesion above the pons; innervation to forehead is b/l so forehead not affected - pts won't be able to close eye tightly so be sure to protect it to prevent foreign bodies/corneal abrasions
26
CNVIII: possible dysfunctions and testing options
- vestibulo-ocular reflex - caloric testing: COWS (nystagmus portion of reaction); inject water into external auditory meatus; cold water = eyes deviate toward injection and nystagmus is opposite; warm water = eyes deviate away from injection and nystagmus is same side
27
CN IX and X
- voice gag reflex tests - 20% of normal people don't have a gag reflex - symptoms = hoarseness, swallowing dysfunction, deviation of uvula - uvula will deviated away from the lesion
28
general definitions: weakness/paresis, paralysis/plegia, hemiparesis, hemiplegia, paraplegia, quadriplegia, incompete quadriplegia
weakness/paresis = diminished strength paralysis, plegia = absence of strength hemiparesis = weakness of one side hemiplegia = paralysis of one side paraplegia = paralysis of legs quadriplegia = paralysis of all extremities incomplete quadriplegia = retention of some upper extremity movement
29
DTRs and levels they test
``` C5/6 = biceps and brachioradialis C7/8 = triceps L3/4 = patellar S1/2 = achilles ```
30
possible changes seen in reflexes
hyporeflexia/areflexia, hyperreflexia symmetric change - could be from polyradiculopahty, peripheral neuropathy, myelopathy asymmetric change - possibly from radiculopathy, central nervous system pathology
31
primitive reflexes
1. frontal release signs 2. grasp, root, snout, suck, palmomental 3. glabellar sign (Myerson sign) - blink = abnormal all these are seen in infants and all (except grasp) can be seen in normal adults
32
cerebellar S&S
1. ataxia - can be caused by cerebellum, peripheral neuropathy, spinal cord, brainstem 2. nystagmus 3. dysdiadochokinesia: decreased rapid alternating movements; can be caused by cerebellum, cerebral, arthritic and extrapyramidal processes; functional
33
sensory dysfunctions
symptoms = paresthesias, dysestesias, numbness, pain, etc. | distinguish using onset, course, location, associated symptoms, hx and meds
34
primary sensory v. cortical/discriminative sensory v. gradient
1. primary sensory = light touch, vibration, proprioception, pain and tempterature 2. cortical/discriminative sensory = graphesthesia, stereognosis, 2 point discrimination, extinction 3. gradient: test distal v. proximal sensation; should have more sensation distally
35
heel walking
- anterior tibialis weakness | - L5 radiculopathy or peripheral neuropathy
36
toe walking
- gastrocnemius or soleus weakness | - S1 radiculopathy or peripheral neuropathy
37
tandem walking
- ataxia | - cerebral, brainstem, cerebellum, spinal cord are all possible sites for lesions causing ataxia
38
Rhomberg test: what systems does it test; implications of positive test
- tests visual, PCML, vestibular systems - at least 2 of the systems have to be working for the test to be negative; so if you do the test w/ eyes open v. shut you can rule in/out a problem w/ the visual system - positive test implicates the cause as either a peripheral neuropathy, spinal cord disease, or a vestibular dysfunction