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67 Cards in this Set

  • Front
  • Back
name the 5 components of the neurological exam, in the order they are generally performed
mental status, cranial nerves, motor/deep tendon reflexes, sensory, gait/coordination
what is the most neurologically relevant component of the mental status exam?
testing speech --> look for fluency, repetition, naming, and comprehension
in anomic aphasia, which of the following are intact: naming ability, fluency, comprehension, repetition
all but naming ability
in broca's aphasia, which of the following are intact: naming ability, fluency, comprehension, repetition? what's it's "cousin" deficit?
comprehension only. it's cousin is transcortical motor aphasia (repetition is spared, fluency is not)
in wernicke's aphasia, which of the following are intact: naming ability, fluency, comprehension, repetition? what's it's "cousin" deficit?
fluency is the only thing spared. it's cousin is transcortical sensory aphasia (repetition is spared, comprehension is not)
in conduction aphasia, which of the following are intact: naming ability, fluency, comprehension, repetition? what's it's "cousin" deficit?
fluency and comprehension are spared. it's cousin is anomic aphasia (all are spared except for naming)
which cranial nerves are tested with visual acuity and fields? pupillary responses? fundascopic exam? extraocular movements?
visual acuity: CN2, pupillary responses: CN2, CN3, fundascopic exam: CN2, extraocular movements: CN 3, CN4, CN6
which cranial nerves are tested by facial sensation? corneal reflex? muscles of facial expression? hearing and vestibular sense?
facial sensation: CN5, corneal reflex: CN5 (afferent), CN7 (efferent), muscles of facial expression: CN7, hearing/vestib: CN8
which cranial nerves are tested by palate elevation and gag reflex? tongue muscles? SCM and trapezius strength?
palate elevation/gag: CN9, CN10, tongue muscles: CN12, SCM and trapezius: CN11
lesions in front of the ___ cause visual deficits in ___, while lesions behind the ___ cause visual deficits that are ___.
lesions in front of the OPTIC CHIASM cause visual deficits in ONE EYE, while lesions behind the optic chiasm cause SIMILAR DEFICITS IN BOTH EYES
where is the lesion? monocular scotoma on the R
R retina, in opposite quadrant of deficit
where is the lesion? monocular visual loss on the R
optic nerve on the R
where is the lesion? bitemproal hemianopia (can't see R visual field in R eye, can't see L visual field in L eye)
optic chiasm
where is the lesion? quadrantanopia in upper L visual field
R Meyer's loop (anterior portion) or lower bank of R calcarine fissure
where is the lesion? quadrantanopia in lower L visual field
R Meyer's loop (posterior portion) or upper bank of R calcarine fissure
where is the lesion? homonymous hemianopia on the L visual field
R optic tract or R optic radiation or R calcarine fissure upper + lower banks
in pupillary reflex testing, the direct response is impaired in lesions of what 4 areas?
ipsilateral optic nerve, pretectal area, ipsilateral parasympathetics (in CN3), pupillary constrictor muscle of the iris
in pupillary reflex testing, the consensual response is impaired in lesions of what 4 areas?
contralateral optic nerve, pretectal area, ipsilateral parasympathetics (CN3), pupillary constrictor muscle
the pupillary reflex is impaired in accommodation testing with which 4 lesions? accommodations is spared in lesions of ___.
accommodation is impaired w/lesions of the ipsilateral optic nerve, ipsilateral parasymptahtetics (in CN3), pupillary constrictor muscle, bilateral lesions of optic tract pathways to cortex. accommodation is SPARED in PRETECTAL lesions.
Horner's syndrome is caused by ___, and is characterized by ___, ___, and ___.
caused by lesions of the CERVICAL SYMPATHETIC TRUNK, and characterized by PUPILLARY CONSTRICTION, ANHYDROSIS, and PTOSIS.
relative afferent pupillary defect (RAPD) is caused by ___ of cranial nerve ___. IIt can be detected only ___. When light is shone in the unaffected eye, ___ constrict(s). When light is shone in the affected eye, ___ constrict(s).
RAPD is caused by an ASYMMETRIC lesion of CN2. It can only be detected IN THE DARK. When light is shone in the unaffected eye, BOTH EYES constrict. When light is shone in the affected eye, the eyes only SLIGHTLY CONSTRICT.
what are 4 causes of anisocoria?
benign essential anisocoria (most common), oculomotor nerve lesion, Horner's syndrome, Adie's pupil
in terms of the pupillary light reflex, how could you differentiate between a L oculomotor nerve lesion and L horner's syndrome?
in L OCULOMOTOR nerve lesion, the L eye will not constrict in response to light directly shone in L eye (DIRECT response affected). in L HORNER'S, the L eye will not constrict in response to light shone in the R eye (consentual response affected).
horner's is more obvious in a ___ (dark/light) room. oculomotor lesions are more obvious in a __ room.
horner's is more obvious in a dark room (impaired pupillary dilation), oculomotor lesions are more obvious in a light room (impaired pupillary constriction).
name 3 causes of light near-dissociation
Argyll Robertson Pupil (neurospyhilis), Parinaud's syndrome (dorsal midbrain syndrome, also associated w/paralysis of up gaze), Adie's pupil (lesion in ciliary ganglion)
name all the players on team rightward gaze
Right PPRF, Right 6th nerve nucleus (R pons); Left frontal eye field; Right 6th nerve, Left MLF, Left 3rd nerve nucleus, Left 3rd nerve
name all the players on team leftward gaze
Left PPRF, Left 6th nerve nucleus (L pons); right frontal eye field; left 6th nerve, right MLF, right 3rd nerve nucleus, right 3rd nerve
describe the defect associated w/right abducens nerve lesion
right eye cannot look right
describe the defect associated w/right abducens nucleus lesion
right lateral gaze palsy (both eyes can't look right) - note: same as right abducens nucleus lesion
describe the defect associated with right PPRF lesion
right lateral gaze palsy (both eyes can't look right) - note: same as right abducens nucleus lesion
describe the defect associated w/left MLF lesion
left INO (left eye cannot look right, right eye has nystagmus on rightward gaze)
describe the defect associated w/lesion in the left MLF and the left abducens nucleus
1 1/2 syndrome --> both eyes can't look left, left eye can't look right, right eye has nystagmus on rightward gaze
describe the characteristic appearance of a patient w/3rd nerve palsy. describe 4th nerve palsy.
3rd nerve palsy: affected eye is down and out and the pupil is too big. 4th nerve palsy: head tilts so that forehead is away from the affected eye, correcting the "up and out" rotation that lesion to CN4 causes.
usually, when a cortical lesion affects the frontal eye fields on the left, the eyes look ___.
LEFT (towards the lesion, away from the paralyzed side). recall that this is caused b/c the rightward gaze center loses tonic input.
what can cause "wrong-way eyes"?
lesion in the pons --> would affect corticospinal tract on opposite side, so the patient would look away from the lesion.
facial sensation can be impaired by lesions of the __ nerve, the ___ nuclei in the ___, or the ascending sensory pathways to the ___ and ___ in the ___.
facial sensation can be impaired by lesions of the TRIGEMINAL nerve, the TRIGEMINAL SENSORY NUCLEI in the BRAINSTEM, or ascending sensory pathways to the THALAMUS and SOMATOSENSORY CORTEX in the POSTCENTRAL GYRUS.
the corneal blink reflex is mediated by postsynaptic connections in the brainstem between the __ and __ nerves, and can be impaired by lesions anywhere in this ciruit
trigeminal and facial (CN5 and CN7)
what can cause facial weakness (3 things)?
lesions of upper motor neurons in contralateral motor cortex, descending central nervous system pathways, lower motor neurons in ipsilateral facial nerve nucleus (CN7). note: upper motor neurons to upper face will spare the forehead, lower motor neurons cause bells palsy type lesions
weber test: normally sound is = in both ears. in conduction loss, it is louder in the ___ ear. in sensorineural loss, the sound is louder in the __ ear.
in conduction loss, sound is louder in ear with decreased hearing. in sensorineural loss, sound is louder in the good ear.
rinne: the sound is normally louder ___ (over the mastoid/in front of the ear) in CONDUCTION hearing loss. and the sounds is normally louder ___ in SENSORINEURAL loss.
in conduction loss, sound is louder over the mastoid. in sensorineural loss, sound is louder in front of the ear.
clinically significant unilateral hearing loss is ___ caused by ____ lesions.
clinically significant unilateral hearing loss is INVARIABLY caused by PERIPHERAL NEURAL or MECHANICAL lesions. (after the hearing pathways enter the brainstem, they cross over at multiple levels and ascend bilaterally to the thalamus and auditory cortex.)
explain the COWS mnemonic
cold opposite warm the same - in HEALTHY AWAKE PEOPLE, cold water in one ear will cause nystagmus w/the fast portion to the opposite side.
in a patient that is not braindead, but is in a coma with damage to the vestibular nuclei, then what will happen when you squirt cold water in their left ear?
eyes will deviate to the left. (recall that it would cause nystagmus to the right in a healthy awake person, so with this lesion, only the slow component remains).
palate elevation and the gag reflex are impaired in lesions involving CN _, CN _, the ___, or the ___ muscles. if the palate elevates to the left (uvula deviated left), it is b/c of weakness in the __.
palate elevation and the gag reflex are impaired in lesions involving CN9, CN10, the neuromuscular junction, or the pharyngeal muscles. if the palate elevates to the left, it is because of weakness in the right (not pulling uvula midline)
fasciculations and atrophy are signs of ___ lesions. unilateral tongue weakness causes the tongue to deviate towards the __ (strong/weak) side. tongue weakness can result from lesions of the ___, the ___, the ___, or the ___.
fasciculations and atrophy are signs of LOWER MOTOR NEURON lesions. unilateral tongue weakness causes the tongue to deviate towards the WEAK side. tongue weakness can result from lesions of the TONGUE MUSCLES, NEUROMUSCULAR JUNCTION, LOWER MOTOR NEURONS of the HYPOGLOSSAL NERVE (12), or UPPER MOTOR NEURONS in the CONTRALATERAL MOTOR CORTEX
explain the corticospinal tract
precentral gyrus (primary motor cortex) --> posterior limb of internal capsuls --> pyramidal decussation in midbrain --> lateral corticospinal tract in spinal cord --> anterior horn, where it synapses on lower motor neuron --> skeletal muscle
involuntary movements and tremors are commonly associated with lesions of the __ or __.
basal ganglia or cerebellum
characteristics of upper motor neuron lesions
weakness, hyperreflexia, increased tone (although acute UMN lesions can be associated w/flaccid paralysis and the increased tone and reflexes develop later on. similarly, atrophy may develop in an UMN lesion over time due to disuse.)
characteristics of lower motor neuron lesions
weakness, atrophy, fasciculatios, hyporeflexia
strength testing: 0/5, 1/5, 2/5, 3/5, 4/5, 5/5
0/5: no contraction. 1/5: muscle flicke, no movement. 2/5: movement possible, but not against gravity. 3/5: can move against gravity but not resistance. 4/5: mvt possible against some resistance, but not normal. 5/5: normal strength.
what are normal reflexes? what is abnormal?
normal is 1-3 (2 being normal, 3 being brisk, 1 being diminished. abnormal is 0 (absent reflex) or 4 (clonus)
name 6 new born infant feflexes
rooting, sucking, moro, grasp, babinski, tonic neck
rooting and sucking reflexes are present ___ and assist in ___. these disappear at around ___.
present at birth, assist in breastfeeding, disappear ~4 mo.s
palmer grasp reflex is present __. persists until __.
present at birth, persiss until 5-6 months of age
the babinski reflex is positive __. fades around __.
positive at birth. fades around 1yr.
the moro reflex is also known as the ___. present __, peaks at ___, and disappears around ___.
moro reflex is the startle reaction (arms spread wide apart when you pull your hands away). present at birth, peaks at 1 month, disappears ~2 months.
the tonic neck reflex, also called ___ is present at ___ and disappears around __.
also called fencing posture (reach arm out to same direction as you turn the head in), the tonic neck reflex is present at 1 month of age and disappears ~4 months (as infants start to learn to sit)
posterior columns are tested by __.
vibration and position sense.
spinothalamic tracts are tested by __.
pain and temperature testing
cortical sensation is tested by __
extinction, 2-point discrimination, graphesthesia, stereognosis.
spinal cord ascending pathways: what tract is at the top (dorsal side) in the center? how about the bottom (ventral side) near the side? how about the very edges?
top: posterior columns (vibration and position). anterolateral tract/spinothalamic tract is front and toward the side. at the very edge is the spinocerebellar tract (dorsal and ventral)
explain the posterior columns pathway
primary somatosensory cortex --> synapse in thalamus: ventral posterior lateral nucleus --> secondary sensory neuron decussates at medulla --> posterior (dorsal) columns
explain the anterolateral (spinothalamic pathway)
primary somatosensory cortex --> synapse in thalamus: ventral posterior lateral nucleus --> secondary sensory neuron ravels through anterolateral pathway (spinothalamic tract) and decussates just before leaving the spinal cord --> exits through dorsal root ganglion
what does the romberg test for? how do you do it?
patient stands together with eyes closed. used to check for sensory ataxia. vision, proprioception, and vestibular function all contribute to the cerebellum. so what happens when you take one out? generally, it's good for detecting problems w/proprioception in particular (vision will be tested w/eye fields etc., vestibular dysfcn is usually accompanied by vertigo)
appendicular coordination cerebellar testing. finger-nose-finger and heel-knee-shin assess __ and rapid alternating movements assess ___
finger-nose-finger assesses DYSMETRIA (decreased ability to aim), and alternating movements assesses DYSDIADOKINESIA (decreased ability to flip b/w muscle groups)
appendicular ataxia is usually caused by lesions of the ___ and associated pathways, while truncal ataxia (Romberg test, gait problems) are usually caused by damage to the __ and associated pathways.
appendicular ataxia usually caused by lesions of the cerebellar HEMISPHERES, truncal ataxia usually caused by damage to the MIDLINE CEREBELLAR VERMIS.
cerebellar dysfunction is always ___.
IPSILATERAL. (same side affected as lesion)