Neuro Flashcards

1
Q

CNS is made of

A

brain and spinal cord

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2
Q

PNS is made of

A

all nerve fibers outside of brain/spinal cord.

  • 12 pairs CNs
  • 31 pairs spinal nerves and branches: sensory and motor
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3
Q

afferent nerve fx

A

sensory afferent nerves carry messages to CNS from sensory receptors

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4
Q

efferent nerve fx

A

motor efferent nerves carry messages from CNS to muscles/glands

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5
Q

PNS fx

A

carries sensory, motor, and autonomic messages that govern internal organs and blood vessels

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6
Q

cerebral cortex is made of?

A
  • outer cerebrum layer of nerve cells

- 2 hemispheres that each have 4 lobes

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7
Q

cerebral cortex fx

A

governs thought, memory, reasoning, sensation, voluntary movement

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8
Q

what are the 4 lobes of each cerebral hemisphere and their functions

A
  1. frontal: personality, behavior, emotion, intellectual function. precentral gyrus initiates voluntary movement
  2. parietal lobe: postcentral gyrus primary center for sensation
  3. occipital lobe: primary visual receptor center
  4. temporal lobe: primary auditory reception center, taste/smell
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9
Q

wernicke’s area location, function?

damage to it results in?

A

in temporal lobe. associated with language comprehension.
damage to wernicke’s in patient’s dominant hemisphere causes receptive aphasia: person can hear sound but it has no meaning, like a foreign language

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10
Q

broca’s area location, function?

damage to it results in?

A

in frontal lobe. mediates motor speech.
damage in the dominant hemisphere causes expressive aphasia: person cannot talk. can understand language and knows what they want to say but when they speak there is only garbled sound.

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11
Q

when does damage to cortical areas occur? what can the damage cause?

A

occurs when the highly specialized neurologic cells are deprived of blood supply like when a cerebral artery becomes occluded (ischemic stroke) or when vascular bleeding occurs (hemorrhagic stroke) or vasospasms.
damage can cause motor weakness, paralysis, loss of sensation, impaired ability to understand/process language.

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12
Q

basal ganglia are what? where? function?

A

large bands of gray matter buried deep in the 2 cerebral hemispheres. they form the subcortical-associated motor system (extrapyramidal system) and help to initiate and coordinate movement and control automatic associated movements of the body (ie arm swing alternating with legs when walking)

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13
Q

what’re some pathologic disorders involving basal ganglia?

A

i dont know lol

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14
Q

thalamus function

A

main relay station. sensory pathways of spinal cord, cerebellum, basal ganglia, and brainstem form synapses on their way to cerebral cortex.
integrating center with connections crucial to human emotion and creativity

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15
Q

pathologic disorders of thalamus?

A

iono

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16
Q

hypothalamus size, location, function

A

size of almond. inferior to thalamus, above midbrain, resting in sella turcica.
links CNS to endocrine system via pituitary.
control center for many PNS autonomic functions:
-sex drive
-temp
-HR/BP
-sleep
-anterior/posterior pituitary gland regulation and coordination of ANS
-stress response
-major respiratory center

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17
Q

pathology of hypothalamus

A
  • gliomas

- hamartomas

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18
Q

what’s cerebellum, where, function

A

it is a coiled structure under occipital lobe.
concerned with motor coordination of voluntary movements, equilibrium (postural balance of the body), and muscle tone.
does not initiate movement: coordinates and smooths it. (playing the piano, swimming, or juggling).
Like autopilot: corrects the voluntary movements but operates entirely below the conscious level.
relays info btwn muscles and areas of cerebral cortex involved in muscle control

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19
Q

whats brain stem? function? where’s brain stem? what it made of?

A
  • central core (lower section) of the brain consisting of mostly nerve fibers
  • continuous with spinal cord
  • Cranial nerves III through XII originate from nuclei in the brainstem
  • fx: Connects motor and sensory tracts from brain to body
  • made of 3 areas: midbrain, pons, medulla
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20
Q

midbrain location and what is it

A

most anterior part of the brainstem that still has the basic tubular structure of the spinal cord.
It merges into the thalamus and hypothalamus.
It contains many motor neurons and tracts.

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21
Q

what is the pons

A

enlarged area containing ascending sensory and descending motor tracts.
has two respiratory centers (pneumotaxic and apneustic) that coordinate with the main respiratory center in the medulla.

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22
Q

what’s the medulla

A

continuation of the spinal cord in the brain that contains all ascending and descending fiber tracts. It has vital autonomic centers (respiration, heart, gastrointestinal function) and nuclei for cranial nerves VIII through XII.
-Pyramidal decussation (crossing of the motor fibers) occurs here

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23
Q

spinal cord

A
  • long, cylindric structure of nervous tissue
  • about as big around as your little finger.
  • occupies the upper two thirds of the vertebral canal from the medulla to lumbar vertebrae L1-L2.
  • white matter, bundles of myelinated axons that form the main highway for ascending and descending fiber tracts that connect the brain to the spinal nerves.
  • mediates reflexes of posture control, urination, and pain response.
  • nerve cell bodies, or gray matter, are arranged in a butterfly shape with anterior and posterior “horns.”
  • vertebral canal continues down beyond the spinal cord for several inches.
  • The lumbar cistern is inside this space and is the favored spot to withdraw samples of cerebrospinal fluid (CSF).
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24
Q

crossed representation

A

CNS pathway. the left cerebral cortex receives sensory information from and controls motor function to the right side of the body, whereas the right cerebral cortex likewise interacts with the left side of the body.

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25
Q

where are sensory receptors? function?

A

Millions of sensory receptors are embroidered into the skin, mucous membranes, muscles, tendons, and viscera. They monitor conscious sensation,
internal organ functions, body position, and reflexes.

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26
Q

sensory pathway

A

Sensation travels in the afferent fibers in the peripheral nerve, through the posterior (dorsal) root,
and into the spinal cord. There it may take one of two routes: the anterolateral or spinothalamic tract, or the posterior (dorsal) columns

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27
Q

spinothalamic tract function, pathway

A

contains sensory fibers that transmit the sensations of pain, temperature, and crude or light touch.
pathway:
The fibers enter the dorsal root of the spinal cord and synapse with a second sensory neuron. The second-order neuron fibers cross to the opposite side
and ascend up the spinothalamic tract to the thalamus.
-Fibers carrying pain and temperature sensations ascend the lateral spinothalamic tract
-crude touch ascend anterior spinothalamic tract.
At the thalamus the fibers synapse with a third sensory neuron, which carries the message to the sensory cortex for full interpretation.

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28
Q

posterior dorsal columns function, pathway

A

These fibers conduct the sensations of:
• Position (proprioception)—Without looking you know where your body parts are in space and in relation to one another.
• Vibration
• Finely localized touch (stereognosis)—Without looking you can identify familiar objects by touch

pathway:
These fibers enter the dorsal root and proceed immediately up the same side of the spinal cord to the brainstem. At the medulla they synapse with a
second sensory neuron and then cross. They travel to the thalamus, synapse again, and proceed to the sensory cortex, which localizes the sensation and
makes full discrimination.

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29
Q

organs absent from sensory cortex

A

heart, liver, or spleen.
You know you have them but you have no “felt image” of it. Pain originating in these organs is referred because no felt image exists in which to have pain. Pain is felt
“by proxy” by another body part that does have a felt image. For example, pain in the heart is referred to the chest, shoulder, and left arm, which were its
neighbors in fetal development. Pain originating in the spleen is felt on the top of the left shoulder.

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30
Q

extrapyramidal tracts are what, do what

A
  • include all the motor nerve fibers originating in the motor cortex, basal ganglia, brainstem, and spinal cord that are outside the pyramidal tract.
  • more primitive motor system.
  • subcortical motor fibers maintain muscle tone and control body movements, especially gross automatic movements such as walking.
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31
Q

upper motor neurons are what, where, function, examples, and diseases

A

-a complex of all the descending motor fibers that can influence or modify the lower motor neurons.
-located completely within the CNS
-convey impulses from motor areas of the cerebral cortex to the lower motor neurons in the anterior horn cells of
the spinal cord
-Examples are corticospinal, corticobulbar, and extrapyramidal tracts
-UMN diseases are stroke, cerebral palsy, and multiple sclerosis.

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32
Q

lower motor neurons where, what, examples, diseases

A
  • located mostly in the peripheral nervous system
  • cell body of the LMN is located in the anterior gray column of the spinal cord, but the nerve fiber extends from here to the muscle
  • LMN is the “final common pathway” because it funnels many neural signals here and provides the final direct contact with the muscles.
  • Any movement must be translated into action by LMN fibers
  • Examples of LMNs are cranial nerves and spinal nerves of the peripheral nervous system.
  • Examples of LMN diseases are spinal cord lesions, poliomyelitis, and amyotrophic lateral sclerosis.
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33
Q

nerve

-peripheral nerve function

A

A nerve is a bundle of fibers outside the CNS.
-The peripheral nerves carry input to the CNS via their sensory afferent fibers and deliver output from the
CNS via the efferent fibers.

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34
Q

reflex definition? types/examples?

A

basic defense mechanisms of the nervous system.

  • involuntary
  • operate below the level of conscious control
  • permit a quick reaction to potentially painful or damaging situations.
  • help the body maintain balance and appropriate muscle tone

4 types:

  1. Deep tendon reflexes (myotatic), e.g., patellar (or knee jerk)
  2. superficial, e.g., corneal reflex, abdominal reflex
  3. visceral (organic), e.g., pupillary response to light and accommodation
  4. pathologic (abnormal), e.g., Babinski (or extensor plantar) reflex.
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35
Q

reflex pathway

A

The fibers that mediate the reflex are carried by a specific spinal nerve. In the simplest reflex tapping the tendon stretches the muscle spindles in the
muscle, which activates the sensory afferent nerve. The sensory afferent fibers carry the message from the receptor and travel through the dorsal root into
the spinal cord. They synapse directly in the cord with the motor neuron in the anterior horn. Motor efferent fibers leave via the ventral root and travel to the muscle, stimulating a sudden contraction.

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36
Q

deep tendon reflex components

A

The deep tendon (myotatic, or stretch) reflex has five components: (1) an intact sensory nerve (afferent); (2) a functional synapse in the cord; (3) an
intact motor nerve fiber (efferent); (4) the neuromuscular junction; and (5) a competent muscle.

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37
Q

cranial nerves are what?

A

Cranial nerves are LMNs that enter and exit the brain rather than the spinal cord.

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38
Q

where to CN 1 AND 2 extend from?

3 thru 12?

A

Cranial nerves I and II extend from the cerebrum; cranial

nerves III through XII extend from the lower diencephalon and brainstem.

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39
Q

what do the 12 pairs of CN supply primarily? except?

A

The 12 pairs of cranial nerves supply primarily the head and neck, except the vagus nerve which travels to the heart, respiratory muscles, stomach, and gallbladder.

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40
Q

spinal nerves where? supply what? names? what type of nerve?

A

The 31 pairs of spinal nerves arise from the length of the spinal cord and supply the rest of the body.
They are named for the region of the spine from
which they exit: 8 cervical, 12 thoracic, 5 lumbar, 5 sacral, and 1 coccygeal.
-“mixed” nerves because they contain both sensory and motor fibers.
-Each nerve innervates a particular segment of the body. -Dermal segmentation is the cutaneous distribution of the various spinal nerves.

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41
Q

dermatome

A

A dermatome is a circumscribed skin area that is supplied mainly from one spinal cord segment through a particular spinal nerve.
-overlap, which is a form of biologic insurance, i.e., if one nerve is severed, most of the sensations can be transmitted by the one above and
the one below.

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42
Q

dermatome landmarks

A
• The thumb C6
1st/2nd fingers C7
4th/5th fingers C8
• The axilla is at the level of T1.
• The nipple is at the level of T4.
• The umbilicus is at the level of T10.
• The groin is in the region of L1.
• The knee is at the level of L4.
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43
Q

autonomic nervous system: somatic vs autonomic fibers

A

The peripheral nervous system is composed of cranial nerves and spinal nerves. These nerves carry fibers that can be divided functionally into two parts:
somatic and autonomic. The somatic fibers innervate the skeletal (voluntary) muscles; the autonomic fibers innervate smooth (involuntary) muscles,
cardiac muscle, and glands.
The autonomic system mediates unconscious activity. its overall function is to maintain homeostasis of the body.

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44
Q

aging and neurologic

A

aging > gradual atrophy > steady loss of neuron structure in the brain and spinal cord > decrease in weight and
volume with a thinning of the cerebral cortex, reduced subcortical brain structures, and expansion of the ventricles

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45
Q

what does neuron loss occurring with aging cause

A

-general loss of muscle bulk (most apparent in the dorsal hand muscles.)
-loss of muscle tone in the face, in the neck, and around the spine
-decreased muscle strength
-impaired fine coordination and agility
-loss of vibratory sense at the ankle
-decreased or absent Achilles reflex
-loss of position sense at the big toe
-pupillary miosis
-irregular pupil shape
-decreased pupillary reflexes.
-reaction time slower in some older people
-touch and pain sensation, taste, and smell may be diminished.
-Muscle strength and agility decrease.
-Muscle tremors may occur in the hands, head, and jaw, along with possible repetitive facial grimacing (dyskinesias).
-progressive decrease in cerebral blood flow and oxygen consumption > in some people, dizziness and a loss of
balance with position change: get up slowly (fall risk + may forget they fell)
-walk more slowly and deliberately. Some survey the ground for obstacles or uneven terrain. Some show a hesitation and a slightly wayward path.

46
Q

this is the worst headache of my life

A

in response to headache question, this needs immediate referral to screen for possible stroke

47
Q

concussion

A

direct blow that causes brain to shift rapidly back and forth inside skull

48
Q

syncope

A

sudden loss of strength, temporary loss of consciousness (faint) caused by lack of cerebral blood flow like in low BP

49
Q

vertigo

A

true vertigo is rotational spinning caused by
neurologic disease in the vestibular apparatus in the
ear or the vestibular nuclei in the brainstem.

50
Q

seizures occur in what condition? characterized by?

A

Seizures occur with epilepsy, a paroxysmal disease
characterized by altered or loss of consciousness,
involuntary muscle movements, and sensory
disturbances.

51
Q

aura

A

subjective sensation that precedes a seizure; it could be auditory, visual, or motor.

52
Q

tremor

A

involuntary shaking, vibrating, or trembling

53
Q

paresis/paralysis

A

Paresis is a partial or incomplete paralysis.
Paralysis is a loss of motor function caused by a lesion in the neurologic or muscular system or loss of sensory innervation.

54
Q

dysmetria

A

the inability to control the distance, power, and speed of a muscular action. clumsy movement with overshooting the mark and occurs with cerebellar disorders or acute alcohol intoxication.

55
Q

paresthesia

A

abnormal sensation (e.g., burning, tingling).

56
Q

dysarthria

A

difficulty forming words

57
Q

dysphasia

A

difficulty with language comprehension or expression

58
Q

why ask what meds? (what kind of neuro meds r we thinking of)

A

Review anticonvulsants and antitremor, antivertigo,

and pain medication.

59
Q

additional aging adult: dizziness when standing up? falls?

A

Diminished cerebral blood flow and vestibular response may increase risk for falls.
Falls risk increases with diagnosis of stroke or dementia, gait and balance disorder, use of assistive devices, history of recent falls

60
Q

additional aging adult: (men) faint while peeing?

A

Micturition syncope.

61
Q

additional aging adult: confusion/change in mental function? sudden or gradual?

A

Memory loss and cognitive decline are early indicators of Alzheimer disease and are mistaken for normal cognitive decline of aging

62
Q

additional aging adult: tremors? worse/relieved by anxiety/alcohol/stress? social or daily?

A

Senile tremor is relieved by alcohol, but this is not a
recommended treatment. Assess if the person is
abusing alcohol in effort to relieve tremor.

63
Q

additional aging adult: vision change? weakness? LOC

A

screening for s/s of stroke

64
Q

equipment needed for neuro exam

A
Penlight
Tongue blade
Cotton swab
Cotton ball
Tuning fork (128 Hz or 256 Hz)
Percussion hammer
65
Q

sequence for neuro exam

A
  1. Mental status
  2. Cranial nerves
  3. Motor system
  4. Sensory system
  5. Reflexes
66
Q

CN 1: when can u not test smell? anosmia is what?

A

One cannot test smell when air passages are occluded with upper respiratory infection or sinusitis.
Anosmia— Decrease or loss of smell occurs bilaterally with tobacco smoking, allergic rhinitis, and cocaine use.
Unilateral loss of smell in the absence of nasal disease is neurogenic anosmia.

67
Q

CN 2: abnormals

A

congenital blindness, refractive error, acquired vision loss from numerous diseases eg stroke, diabetes, trauma to globe or orbit

  • defect/absent central vision
  • defect in peripheral vision, hemianopsia
  • absent light reflex

increased ICP, glaucoma, diabetes

  • papilledema (also optic atrophy)
  • optic atrophy
  • retinal lesions
68
Q

CN 3,4,6: ptosis, pupils, nystagmus, strabismus

A

Ptosis (drooping) with MG, dysfx of cn3, or Horner syndrome.
Increasing ICP causes sudden, unilateral, dilated, nonreactive pupil.
Nystagmus with disease of vestibular system, cerebellum, or brain stem.
Strabismus deviated gaze or limited movement

69
Q

CN 5: strength, pain, touch

A

Decreased strength one or both sides. asymmetric jaw movement. pain clenching teeth.
Decreased or unequal sensation. Stroke: sensation of face and body lost on opposite side of lesion

70
Q

CN 7: muscle weakness

A

Muscle weakness shown with:

  • flattening of nasolabial fold
  • drooping of one side of face
  • lower eyelid sagging
  • escape of air from only one cheek that is pressed in
  • loss of movement and asymmetry of movement occur with both CNS lesions (stroke: lower face affected one side) and PNS lesions (Bell palsy: whole face affected one side)
71
Q

CN 9 and 10: palate movement, stroke, voice

A

Absence or asymmetry of soft palate movement or tonsillar pillar movement.
following stroke, dysfx in swallowing may increase risk for aspiration.
Hoarse or brassy voice occurs with vocal cord dysfx, nasal twang with weakness of soft palate

72
Q

CN 11 abnormalities

A

Atrophy. Muscle weakness or paralysis occurs with a stroke or following injury to the peripheral nerve (e.g., surgical removal of lymph nodes).

73
Q

muscle atrophy, hypertrophy

A

Abnormally small muscle with a wasted appearance; occurs with disuse, injury, LMN disease such as polio, diabetic neuropathy.

Hypertrophy— Increased size and strength; occurs with isometric exercise.

74
Q

flaccidity, spasticity

A

Flaccidity—
Decreased resistance, hypotonia occur with peripheral weakness.

Spasticity and rigidity—Types of increased resistance that occur with central weakness

75
Q

possible involuntary movements

A

Tic, tremor, fasciculation, myoclonus, chorea, and athetosis

76
Q

RAM abnormals

A

Lack of coordination. Slow, clumsy, and sloppy response is termed dysdiadochokinesia and occurs with cerebellar disease.

77
Q

past pointing

A

constant deviation to one side.

78
Q

intention tremor

A

reaching to a visually directed object.

79
Q

worsening coordination when eyes are closed with finger to nose?

A

Worsening of coordination when the eyes are closed occurs with cerebellar disease or alcohol intoxication.

80
Q

heel falls off shin?

A

cerebellar disease

81
Q

ataxia

A

Uncoordinated or unsteady gait. may appear only on hell-toe.

82
Q

inability to tandem walk?

A

sensitive for an upper motor neuron lesion such as multiple sclerosis and for acute cerebellar dysfunction such as alcohol intoxication.

83
Q

pos romberg when?

A

positive Romberg sign occurs with cerebellar ataxia (multiple sclerosis, alcohol intoxication), loss of proprioception, and loss of vestibular function.

84
Q

what to note for sensory loss?

A

Note if the topographic pattern of sensory loss is distal (i.e., over the hands and feet in a “glove and stocking” distribution) or if it is over a specific dermatome.

85
Q

hypoalgesia, analgesia, hyperalgesia

A

Hypoalgesia— Decreased pain sensation.
Analgesia—Absent pain sensation.
Hyperalgesia— Increased pain sensation.

86
Q

hypoesthesia, anesthesia, hyperesthesia

A

Hypoesthesia— Decreased touch sensation.
Anesthesia— Absent touch sensation.
Hyperesthesia— Increased touch sensation.

87
Q

loss of vibration sense indicates?

A

Loss of vibration sense occurs with peripheral neuropathy (e.g., diabetes and alcoholism). Often this is the first sensation lost. Peripheral neuropathy is worse at the feet and gradually improves as you move up the leg, as opposed to a specific nerve lesion, which has a clear zone of deficit for its dermatome

88
Q

problems with tactile discrimination indicate?

A

lesions of the sensory cortex or posterior column.

89
Q

astereogenesis

A

Inability to identify object correctly. Occurs in sensory cortex lesions (e.g., stroke).

90
Q

inability to distinguish numbers? (graphesthesia)

A

lesions of the sensory cortex.

91
Q

An increase in the distance it normally takes to

identify two separate points occurs with?

A

sensory cortex lesions

92
Q

stimulus is extinguished on one side during 2 simultaneous touch? (extinction)

A

the stimulus is extinguished on the side opposite the cortex lesion.

93
Q

point location problem?

A

With a sensory cortex lesion, the person cannot localize the sensation accurately, even though light touch sensation may be retained.

94
Q

clonus? hyperactive with sustained clonus?

A

a set of rapid, rhythmic contractions of the same muscle.
repeated reflex muscular movements. A hyperactive reflex with sustained clonus (lasting as long as the stretch is held) occurs with UMN disease.

95
Q

hyperreflexia

A

the exaggerated reflex seen when the monosynaptic
reflex arc is released from the usually inhibiting influence of higher cortical levels. This occurs with upper motor neuron lesions (e.g., stroke).

96
Q

hyporfeflexia

A

the absence of a reflex, is a lower motor neuron problem. It occurs with interruption of sensory afferents or destruction of motor efferents and anterior horn cells (e.g., spinal cord injury).

97
Q

absent superficial reflexes

A

Superficial reflexes are absent with diseases of the pyramidal tract (e.g., they are absent on the contralateral side with stroke).

98
Q

when do you test sensory for Facial Nerve

A

only when damage is suspecte do u test taste

99
Q

when do u test temperature for sensory function

A

if pain response to pinprick is abnormal only because the tracts are similar

100
Q

abdominal reflexes

A

upper: T8-T10
lower: T10-T12
normal: ipsilateral abd contraction with umbilicus moving toward strike area

101
Q

cremasteric reflex

A
  • not routinely tested
  • males
  • strike inner thigh, ipsilateral testicle should contract
  • absent in both UMN/LMN lesions
102
Q

plantar reflex

A

-draw an upside down J on lateral side of foot in toward ball of foot
-normal: plantar flex toes, inversion and flexion of forefoot
-Except in infancy, the abnormal response is dorsiflexion of the big toe and fanning of all toes, which is a positive Babinski sign, also called “upgoing toes” This occurs
with UMN disease of the corticospinal (or pyramidal) tract.

103
Q

aging: Absence of a rhythmic reciprocal gait pattern is seen in

A

parkinsonism and hemiparesis

104
Q

aging: neurologic changes

A

changes may be subtle. consider all even subtle changes, including complacency in previously combative pt

105
Q

weak hand grips

A

occurs in upper and lower motor neuron disease and with local hand problems (arthritis, carpal tunnel syndrome).

106
Q

pronator drift

A

downward unilateral drift and turning in of the forearm that occurs with mild hemiparesis.

107
Q

Any abnormal posturing, decorticate rigidity, or decerebrate rigidity indicates

A

diffuse brain injury

108
Q

sudden unilateral dilated and nonreactive pupil in brain injured pt

A

ominous.
Cranial nerve III runs parallel to the brainstem. When
increasing intracranial pressure pushes the brainstem down (uncal herniation), it puts pressure on cranial nerve III, causing pupil dilation.

109
Q

cushing reflex

A

shows signs of increasing intracranial pressure: BP sudden elevation with widening pulse pressure; pulse—decreased rate, slow and bounding.

110
Q

aging adult changes

A

Aging adult
Cranial nerves mediating taste & smell not usually tested
Decrease in muscle bulk most apparent in hand
Senile tremors occasionally occur; these benign tremors include an intention tremor of hands, head nodding & tongue protrusion
Dyskinesias may accompany senile tremors
Gait may be slower, more deliberate than in younger person
RAM, may be difficult to perform
Plantar reflex may be absent or diminished
After 65 years of age, loss of sensation of vibration at ankle malleolus common
Tactile sensation may be impaired; may need stronger stimuli for light touch & pain
DTRs less brisk