Neurological System Flashcards

1
Q

frontal lobe is responsible for:

A

primary motor cortex:
personality
expressive speech (Broca’s area)
judgement & decision-making
abstract thought
concentration
temper

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

frontal lobe impairment causes:

A

contralateral weakness
inattention
apathy
poor inhibition
personality change
Broca’s aphasia (expressive deficits)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

parietal lobe is responsible for:

A

gross sensation (touch, pressure)
fine sensation (texture, weight, size, shape)
sensory homonculus
language
spatial & visual perception

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

parietal lobe impairment causes:

A

L side: agraphia, alexia, agnosia (language comprehension)
R side: dressing & constructional apraxia, anosognosia (no insight)
contralateral sensory deficits: impaired language, taste & comprehension

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

temporal lobe is responsible for:

A

primary auditory processing & olfaction
behavior
language reception (Wernicke’s area)
understanding
Long term memory
interpret nonverbals of others

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

temporal lobe impairment causes:

A

learning deficit
antisocial/aggressive
Wernicke’s aphasia
difficulty w/ facial recognition, memory & categorizing objects

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

occipital lobe is responsible for:

A

vision & 3D
recognize size, shape & color
judging distance

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

occipital lobe impairment causes:

A

impaired eye muscle movement
visual deficits
decreased color recognition
read/write deficits
homonymous hemianopsia
cortical blindness w/ bilat. lobe involved

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

hippocampus location & function

A

(lower temporal lobe)
learning language
form/store new personal memories
declarative memory
sending memory to appropriate areas of cerebral hemisphere

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

basal ganglia function

A

voluntary movement
regulate autonomic movement, posture & mm tone
(includes caudate, putamen, globus, pallidus, substantia nigra, subthalamic nuclei)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

diseases of dysfunctional basal ganglia

A

Parkinson’s
Tourette’s
Huntington’s
ADD
OCD
addictions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

amygdala location & function

A

(in temporal lobe, next to hippocampus)
Emotional and social processing
Fear/pleasure response, arousal, memory processing, form emotional memories

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

hypothalamus function

A

receive/integrate info from autonomic NS
hormone regulation
controls hunger, thirst, sex, sleep
regulate body temp, adrenal glands, pituitary glands

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

subthalamus location & function

A

between thalamus & hypothalamus
regulates movement from skeletal muscle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

epithalamus/pineal gland function

A

secretes melatonin for circadian rhythm
regulates some motor pathways & emotions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

cerebellum function

A

balance, posture & complex muscle movements
integration, coordination & execution of multi-joint movements
regulates mm contractions (initiation, timing, sequencing, force)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

pons function

A

helps regulate respiration rate
associated w/ head orientation to visual/auditory stimuli
includes CN 5-8 origins

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

medulla oblongata function & wht/gry matter distribution

A

influence autonomic activity (RR & HR)
reflex center for vomiting, coughing, sneezing
outer white matter, inner gray matter

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

What is responsible for exchanging nutrients between the CNS & vascular system?

A

blood/brain barrier

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

3 Meninges Layers & 3 spaces between

A

[skull]
-epidural space
dura mater (outer)
-subdural space
arachnoid mater (middle)
-subarachnoid space w/ CSF
pia mater (inner)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

PNS: how many cranial nerves?
how many spinal nerves? (cervical, thoracic, lumbar, sacral, coccygeal)

A

12 CN
8 cervical
12 thoracic
5 lumbar
5 sacral
1 coccygeal

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

sympathetic NS: hormone, affect on BP, HR & blood flow

A

norepinephrine
inc. HR, BP & blood flow to skeletal mm

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

parasympathetic NS: hormone & affect on HR, BP & digestion; which CN affected (4 total)

A

acetylcholine
dec/normalized HR, BP & digestion
oculomotor (3), facial & glossopharangeal (7, 9, taste) & vagus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

Name 3 early embryo layers

A

ectoderm: brain components
mesoderm: vertebrae/skull, dermis, skeletal mm
endoderm: organ development

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
upper motor neurons: cell body origin/termination where do they cross? where do they synapse w/ LMN?
origin: cerebral cortex termination: brainstem/spinal cord cross: medulla LMN synapse: anterior horn of SC
26
UMN Lesions = which diseases?
MS SCI Parkinsons CVA/stroke TBI/head trauma ALS
27
UMN lesion characteristics
spastic weakness loss of autonomic control clonus paralysis hyperreflexia
28
lower motor neurons: cell body origin of cranial nerves & spinal nerves
CN: brainstem spinal nerves: anterior horn of S.C.
29
LMN lesions = what diseases?
muscular dystrophy polio myasthenia graves ALS, Guillan Barre peripheral nerve injury
30
LMN lesion characteristics
hypotonia hyporeflexia paralysis atrophy loss of coordination
31
temporary nerve damage due to pressure
neuropraxia
32
prolonged nerve pressure causes muscle atrophy & axon degeneration (can be permanent)
axonotmesis
33
nerve axon/sheath damaged; can require surgery
neurotmesis
34
when peripheral nerve is cut & parts of axon distal to transaction point are disconnected from central neuron
Wallerian degeneration
35
PT tx: reduce return of primitive reflex patterns of movement (post CVA) -stimulate return of normal tone/posture
Brunnstrom approach
36
PT tx: focusing on normal movement without compensations (often w/ UMN lesions)
neurodevelopmental therapy (NDT)/ Bobath technique
37
progressive degenerative organic brain syndrome that destroys neurons of cerebral cortex (frontal lobe first) w/ plaques
Alzheimer's Disease
38
s/s: memory & behavioral deficits (no cure)
Alzheimer's Disease
39
Name 4 types of Non-Alzheimer's dementia
Lewy body dementia vascular dementia head trauma dementia substance-induced dementia
40
inflammation of meninges (acute or chronic that affects different layers) -which of the 2 is more fatal?
meningitis bacterial: (fatal) disrupted blood-brain barrier viral: more common
41
s/s: high fever ,chills, photophobia, severe HA, vomit, neck stiffness, drowsy, stupor, seizures, coma
meningitis
42
inflammation of parenchyma of brain tissue due to viral invasion
encephalitis
43
brain damage due to ischemia (embolus blockage) or hemorrhage stroke (aneurysm)
cerebrovascular accident, CVA
44
s/s: HA, weakness on 1 side of face/body, slurred speech, blurred vision, sudden flaccidity, spasticity in 2-3 days
CVA
45
group of rare, prion degenerative neuro disorders w/ rapid progressive dementia
Creutzfeldt-Jacob Disease
46
numerous neurons in brain fire at the same time, leading to large burst of electrical energy (Types: absence/petit mal, atonic, myoclonic, tonic clonic/grand mal)
epilepsy/seizure disorders
47
hereditary progressive, degenerative disease affecting 4th chromosome
Huntington's Disease
48
s/s: mm rigidity, tremors, slow movement, myoclonus, chorea (involuntary jerky/uncoordinated, hallucinations)
Huntingon's Disease
49
autoimmune, demyelinating neuro disorder of UMNs in CNS b/c plaques/lesions in brain
multiple sclerosis
50
s/s: blurred vision, numb/tingling, cognitive deficits, heat sensitivity, mm weakness, fatigue, unsteady gait
multiple sclerosis
51
UMN disease affecting basal ganglia (voluntary movement) d/t deficient dopamine & excess ACH
Parkinson's Disease
52
s/s: tremors, posture changes, masklike facial expression, slow/soft speech, rigidity, difficulty initiating movement, shuffling gait, bradykinesia, cognitive impairment, mm atrophy, fatigue
Parkinson's Disease
53
LMN disorder w/ autoimmune response which motor neurons spared during original poliomyelitis infection become overused/overstressed
Post-Polio syndrome
54
PT tx: reduce excess physical activity w/ low-impact aerobics & strengthening (don't fatigue mm); energy conservation
Post-polio syndrome
55
UMN disorder causing partial/complete paralysis (usually d/t trauma)
Spinal Cord Injury
56
s/s: lesion to C4/C6- quad/tetraplegia, T6- paraplegia, L1- paraplegia autonomic dysreflexia
spinal cord injury
57
external injury to head that damages brain tissue (usually a fall or MVA); UMN lesion
traumatic brain injury
58
s/s: loss of consciousness, dec. memory, HA, dizzy, behavior changes, mood swing, nausea/vomit, seizures, coma
TBI
59
2 measurement scales for TBI
Glasgow Coma Scale: for acute injury, rate consciousness level Rancho Los Amigos Scale: determine prognosis
60
collection of blood between skull & dura mater; large, arterial & develops fast
epidural hematoma
61
collection of blood between dura mater & arachnoid mater; slow developing, venous
subdural hematoma
62
temporary, unilateral facial paralysis d/t trauma (affects CN 7- facial)
Bell's Palsy
63
s/s: asymmetrical facial appearance w/ dropping eyelid/mouth
Bell's Palsy
64
peripheral nerve disease affecting motor, sensory & autonomic systems causes: diabetes mellitus, guillian-barre, alcoholism, autoimmune disease
neuropathy
65
immune system attacks & demyelinates peripheral nerves; triggered by infection of trauma (LMN disease)
Guillian Barre Syndrome
66
s/s: LE mm weakness that spreads to UE; no DTRs, flaccidity; greatest weakness at 3 wks
Guillian Barre syndrome
67
intense attacks of pain along nerve distribution of CN V- trigeminal; caused by viral infection
trigeminal neuralgia /tic douloureux
68
progressive, degenerative disease of UMN & LMN; unknown cause & intact sensory system
Amyotrophic Lateral Sclerosis (ALS)/ Lou Gehrig's
69
s/s: gradual onset but progressive mm weakness (cachexia), spasticity, involuntary movement, hyperreflexia, fatigue, dysarthria
ALS/Lou Gehrig's
70
neural tube defect that prevents brain formation
Anencephaly
71
rare developmental deficit where cerebellum protrudes through foramen magnum & puts pressure on S.C., cerebellum & cerebrum
Arnold-Chiari Malformation
72
wide range of developmental disorders causing impaired social interaction, delayed speech development, repetitive behaviors, sensitivities to stimuli
Autism Spectrum Disorder
73
any injury to infant brain by congenital abnormalities before/during/immediately after birth ex: hypoxia, mechanical trauma etc
Cerebral Palsy
74
s/s: physical, musculoskeletal, behavioral and cognitive disorders: small jaw/eyes, cleft palate, flat nasal bridge, microencephaly, mental/growth retardation, poor attention & social skills, hyperactivity, etc
fetal alcohol spectrum disorder
75
developmental defect in forebrain of embryo/fetus
holoprosencephaly
76
dorsal column region: proprioception of UEs, trunk & neck; detect vibration, 2 point discrim., graphesthesia
fasciculous cuneatus; outer region
77
dorsal column region: proprioception of LEs and trunk
fasciculous gracilits; medial region
78
dorsal column: which direction, where crosses, detects what
ascending sensory tract crosses in pons deep sensation: proprioception, kinesthesia, vibration, combined deep sensation
79
spinothalamic tract: which direction, where crosses, detects what
ascending sensory tract crosses 2-4 levels above S.C. superficial sensation: light touch/pressure, pain, temperature
80
corticospinal tract: which direction, where crosses; movement per lateral & medial tracts
descending motor tract crossses in brainstem lateral: contralateral voluntary fine movement medial: contralateral voluntary discrete/skilled movement
81
Name 3 other ascending/sensory tracts
spinoreticular tract spinotectal tract spinocerebellar tract
82
Name 4 other descending /motor tracts
tectospinal tract vestibulospinal tract reticulospinal tract rubrospinal tract
83
lesion of hemisection of SC ipsilateral paralysis of corticospinal tract ipsilateral sensory loss at dorsal column contralateral sensory loss at spinothalamic
Brown-Sequard Syndrome
84
loss of motor function (corticospinal) below lesion loss of superficial sensation below lesion (dosal columns preserved)
Anterior Cord Syndrome
85
spinal cord syndrome: occur from hyperextension injury to cervical or degenerative narrowing of spinal canal affect UE more than LE
Central Cord Syndrome
86
compression of posterior spinal artery loss of dorsal column function motor function preserved
Posterior Cord Syndrome
87
spinal cord syndrome: a LMN injury w/ areflexic bowel/bladder, saddle anesthesia & variable LE paralysis
Cauda Equina Injury
88
spinal cord syndrome: (T12-L2 injury) UMN & LMN deficits w/ loss of bowel/bladder, saddle anesthesia & LE motor weakness
Conus medullaris injury
89
s/s: high BP, low HR, diaphoresis, anxiety, stimuli sensitivity
autonomic dysreflexia `
90
place where the anterior and posterior circulation systems of the brain converge to provide collateral blood flow
Circle of Willis
91
2 diseases that use lumbar puncture to diagnosis
Meningitis Encephalitis
92
PT tx for which disease? strength, stretch, aerobic ex, low temp aquatic therapy, functional e-stim, balance, coordination
multiple sclerosis
93
PT tx for which disease? limited physical activity, energy conservation, low-impact aerobics/strength, use AD, (no fatiguing mm)
Post-polio syndrome
94