Neural Bases of Speech and Language Test 1 Flashcards

1
Q

the study of the anatomy, physiology, and pathology of the nervous system

A

Neurology

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2
Q

study of structure

A

anatomy

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3
Q

the study of the nervous system’s structure

A

neuroanatomy

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4
Q

study of function

A

physiology

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5
Q

the study of the nervous system’s functions

A

neurophysiology

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6
Q

study of diseases

A

pathology

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7
Q

the study of nervous system dieases

A

neuropathology

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8
Q

a series of organs, brain, spinal cord, and all the nerves that go into your muscles

A

nervous system

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9
Q

brain and spinal cord

A

central nervous system

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10
Q

everything to the outside of the brain, nerves and cranial nerves

A

peripheral nervous system

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11
Q

the removal or repair of structures that impair normal nervous system functioning

A

neurosurgery

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12
Q

the use of radiation therapy for nervous system tumors

A

neuroradiology

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13
Q

normal and pathological development of the nervous system

A

neuroembryology

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14
Q

to speak the language of neurologists and better communicate with them. we might be working with neurologists in a hospital and it will make things easier if you can both understand each other.

A

need for neurological training in SLP’s

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15
Q

to choose appropriate testing instruments placed on neurological injury. to predict problems patients are likely to have. to document change/efficacy of treatments. to plan effective treatment,

A

need for neurological training in SLP’s

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16
Q

a universal human experience, sometimes permanent or transient that affects the health and functioning

A

disability

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17
Q

encephalitis/meningitis (brain infection/ infection in membranes that surround brain)

A

Inflammatory diseases

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18
Q

Huntington disease (inherited diseases that eventually causes death) (your brain cells die/ “atrophies” which means to “waste away”

A

Systematic CNS atrophies

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19
Q

Parkinson disease (extrapyramidal tract is not working correctly and that tract affects movement)

A

Extrapyramidal disorders

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20
Q

Alzheimer disease (progressive neurological disorder (keeps going and doesn’t stop/no cure))

A

other degenerative diseases

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21
Q

Multiple sclerosis (nerves are covered in Myelin to keep electrical impulses in) ( in this diseases myelin is not on nerves correctly and has so nerves have gone array)

A

demyelinating CNS diseases

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22
Q

Epilepsy, Stroke (sudden)

A

Episodic/Paroxysmal disorders

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23
Q

an example of this group of believers called radical localists. they believe that certain areas of the brain and only certain areas perform certain or specific mental functions.

A

Phrenology

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24
Q

these people believe certain parts of the body were responsible for certain mental functions

A

radical localists and localists

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25
these people believe certain parts of the body were responsible for certain functions as they are interconnected and work cooperatively.
connectionists
26
these people believe that the whole brain is involved in mental functioning
holists
27
viewing the anatomy of the brain (CT, MRI, Angiography)
structural imaging
28
viewing the physiology of the brain (PET, EGG, and MEG)
functional imaging
29
Method of imaging the structure of the vascular system Iodine injected into this system X-rays used to image the vascular system
angiography
30
the location of brain activity when a stimulus is introduced
spatial resolution
31
the time between a stimulus being presented and the brain’s response to that stimulus
temporal resolution
32
divides structure into left and right portions
sagittal section
33
divides structure into front and back portions
coronal section
34
divides structure into upper and lower portions
transverse section
35
from a high position
superior
36
from a low position
inferior (caudal)
37
toward the stomach
anterior (ventral)
38
toward the back
posterior (dorsal)
39
away from the body's midline
lateral
40
toward the body's midline
medial
41
point nearest limb's attachment
proximal
42
point farthest from limb's attachment
distal
43
toward the outer surface
peripheral
44
toward the center
central
45
on the same side
ipsilateral
46
on the opposite side
contralateral
47
bringing structures together
adduct
48
moving structures apart; taken away/kidnapped
abduct
49
bending a joing
flexion
50
straightening out a joing
extension
51
face/ventral surface is up
supine
52
face-ventral surface is down
pronate
53
structures that can be seen through human eyes
anatomical approach
54
lies inferior to cerebral hemispheres and continuous with brainstem. consists of medulla, pons, and midbrain. controls basic life functions such as breathing, heartbeat etc., has motor and sensory pathways that run between brain and spinal cord.
brainstem
55
lies posterior to pons. involved in coordination and precision of fine motor movements.
cerebellum
56
includes thalamus, subthalamus, hypothalamus, and epithalamus
diencephalon
57
relay station for sensory fibers
thalamus
58
regulates and coordinates motor functions
subthalamus
59
regulates body functions (body temperature)
hypothalamus
60
regulates sleep-wake cycle, genital development and optic reflexes
epithalamus
61
controls higher cortical functions such as cognition and language, planning motor function and interpreting sensory experiences
cerebral hemisphere
62
Housed in the spinal or vertebral column with 32 to 34 boney segments Densely packed with motor and sensory fibers Spinal nerves exit and course to the body structures
spinal cord
63
consists of 12 pairs of cranial and 31 pairs of spinal nerves
peripheral nervous system
64
Transfer motor (body movement), sensory (temp., touch), special sensory (vision, hearing, taste, smell) and parasympathetic (regulates glands & organs) information
cranial nerves
65
8 cervical, 12 thoracic, 5 lumbar, 5 sacral and 1 coccygeal Motor and sensory information Mediates reflexes
spinal nerves
66
general senses such as touch, pain, pressure, vibration, temp. special senses such as vision, hearing and balance
somatosensory system
67
general senses such as stretch, pain, temp., nausea, hunger, and irritation from internal organs. Special sense such as taste and smell
visceral sensory system
68
Involved body functions that happens automatically and without conscious control Sympathetic - “fight-or-flight” Parasympathetic - “rest-and digest” Enteric - manages gastrointestinal system
autonomic nervous system
69
Voluntary and conscious control of skeletal muscle movements Includes 12 cranial and 31 spinal nerves
somatic nervous system
70
forms as a single fertilized egg and develops into complex organism
human being
71
human chromosomes
46 (23 pairs)
72
divide and duplicate through mitosis. 4 stage process - mother cell divides and forms two genetically identical daughter cells.
somatic cells
73
error during mitosis: whole chromosome deletion
turner syndrome
74
error during mitosis: partial chromosome deletion
cri-du-chat syndrome
75
error during mitosis: addition of chromosome
trisomy
76
week 1. sperm penetrates ovum to form zygote. the zygote begins to divide to form a morula. when zygote enters uterus and differentiates into outer and inner cells.
germinal stage
77
weeks 2-8. blastocyte implants into wall of uterus. beginning layers of the embryo: endoderm - gut, liver, and lungs. mesoderm - skeleton, muscles, kidneys, blood, and heart. ectoderm - skin and nervous system. neurodevelopment of central nervous system.
embryonic stage
78
weeks 3-7. period when neural tube is formed. 3rd week: ectoderm thickens to form neural plate.4th week: neural plate wraps around to form the neural tube (process called neurulation) 6th week: ends of neural tube close. brain and spinal cord will develop out of the neural tube
dorsal induction
79
encephalocele: when parts of the brain protrude from the skull. anencephaly: brain development ceases at brainstem; child without cerebral hemispheres. spina bifida: cyst on back that may or may not involve the spinal cord.
dorsal induction neural tube defects
80
months 2-3. period when the face and brain develop out of the superior end of the neural tube.Brain divisions include the following: 1. Prosencephalon (Forebrain) - Telencephalon & Diencephalon 2. Mesencephalon (Mid brain) 3. Rhombencephalon (hind brain) - myelencephalon 4. Metencephalon
ventral induction
81
Holoprosencephaly: failure of brain cleavage Alobar form = no cleavage at all resulting in no distinct cerebral hemispheres; no corpus callosum Semilobar form = some cleavage and development of right and left hemispheres, but incomplete; no corpus callosum Lobar form = least severe; brain looks normal, but abnormal connections between hemispheres
ventral induction defects
82
months 3-4.Neurogenesis = the birth of new neurons New neurons will become the gray and white matter of the cerebral hemispheres Initially born out of spinal cord and brainstem; later the whole periventricular area Interruptions in neural proliferation may result in microcephaly where children have abnormally small heads/brains
neural proliferation
83
months 3-5.New neurons move in wavelike fashion to their correct position in the cerebral hemispheres. A chemical reelin signals neurons where to stop At about 20 weeks GA, process stops and 6 layers of the cerebral cortex are established Cells cluster to form - hills (gyri) & valleys (sulci). Four lobes and its function develop
neuronal migration
84
Schizencephaly: clefts in the cerebral hemispheres. Lissencephaly: smooth brain that lacks characteristic sulci and gyri. Both conditions due to lack of reelin leading to a failure of neurons to migrate to proper places
neuronal migration defects
85
5 months to years. Once neurons arrive at intended spot, they sprout dendrites and axons Synapses begin to form between neurons Process known as synaptogenesis Synaptic pruning eliminated unneeded connections Failure in this stage can lead to polymicrogyria; too many guru in the cerebral hemispheres
cortical organization and synapse formation
86
birth to years after birth.Neuron axons are coated with myelin during this stage Process reaches its peak about 1 year after birth This is when infants gain greater controls of their bodies and begin to develop the ability to communicate verbally Failure in this stage may result in hypomyelination, a reduced ability to form myelin resulting in intellectual disability, etc.
myelination
87
Flexion and extension of trunk begin at a GA of 10–12 weeks Reflexes (e.g., startle) begin at GA of 10 weeks Movement of head and limbs at GA of 12 weeks Facial behaviors such as sucking, swallowing etc. emerge in second trimester Third trimester: above become more coordinated
functional development of the infant brain fetal behavior
88
begins at back of the brain and moves to the front; prefrontal cortex last area to be pruned
synaptic pruning
89
two or more atoms held together by a chemical bond
molecules
90
carbohydrates. stored for energy to the cellular functions
simple sugars
91
fats. responsible for cell architecture. ex: cell membrane. nervous system - contributes to myelin
fatty acids ( or lipids)
92
amine + carboxylic acid. brain - glutamate and gamma - aminobutyric acid (GABA). important for excitatory and inhibitory neurotransmitter
amino acids
93
large molecules for building body structure. DNA and RNA.
nucleotides
94
selectively permeable barrier/protector
membrane
95
stores and delivers proteins
golgi apparatus
96
contents of cell
cytoplasm
97
produce energy for the cell
mitochondrion
98
genetic control center
nucleus
99
produce ribosomes
nucleolus
100
produce proteins
ribosomes
101
cell division and microtubule formation
centrioles
102
digest cell debirs and bacteria
lysosome
103
cell framework and movement of cell parts
microtubules
104
rough ER produces proteins; smooth ER produces fatty acids, calcium, enzymes
ER
105
cells with specialized projection that transfers information throughout the body through electrochemical process
neuronal cells
106
glue cells
glial cells
107
neurons consist of:
cell body
108
nerve fibers
neurites
109
tree like structure that receives signals and pass to the cell body
dendrites
110
conducting signals away from the cell body
axons
111
mediates transmission excitatory/inhibitory modulatory
chemical messenger
112
motor signals from CNS to PNS (descending)
efferent communication
113
sensory signals from PNS to CNS (ascending)
afferent communication
114
active and passive
transport
115
imbalance
gradient
116
step 1. polarization. step 2. chemical transmission, depolarization. step 3. repolarization
neuronal firing
117
rest state: 1. concentration gradient. Na and K imbalance 2. charge gradient. More negative charge inside. Action (energy) potential
polarization
118
chemical firing of the neuron occurs at synapse. Neurotransmitters (presynaptic membrane (released in synaptic cleft
chemical transmission
119
chemical firing of the neuron occurs at _______
synapse
120
neurotransmitters released in ______ _____
synaptic cleft
121
The equaling of the gradients (both electrical and concentration) Protein channels open and allow NA+ into cell using passive transport
depolarization
122
Re-establishing of the gradients (both electrical and concentration) by the Na/K pump (active transport)
repolarization
123
abnormal growth of nervous system
neoplasms
124
slow growing and do not spread
benign brain tumors
125
grown quickly and spread to other parts
malignant brain tumors
126
autoimmune disorder of unknown cause. Pins and needles. Issues with walking, balance, speech and swallowing.
multiple sclerosis
127
* 12-18 inch in length and ¼ to ½ inch in diameter * Communication superhighway for motor or efferent (from the brain to the body) and sensory supplies (from the body to the brain) * Extends from the bottom of the brainstem to the vertebral column * Bony covering – vertebral column and three layers of meninges
spinal cord
128
motor and sensory information (GSE and GSA) to and from the dorsal or posterior part of the body
dorsal ramus/branch
129
* Inflammation of spinal cord * Cause by virus, bacteria, parasites and any toxic agents (ex: led poisoning) * Loss of motor function or sensory or both
myelitis
130
* Superior end of the spinal cord; anterior to cerebellum * Contains the ascending and descending tracts as well as major nuclei of cranial nerves * Medulla, pons and midbrain
brainstem
131
* Lowest part of the brain stem and lies between the spinal cord and pons.
the medulla
132
consists of descending and ascending tract (majority) and olive (olive nucleus) – integrates signals from the cerebellum and spinal cord for coordination and learning.
pyramids
133
(IX, X, XI, and XII) – 9 – glossopharyngeal, 10 – vagus, 11 – accessory, 12 – hypoglossal; swallowing, respiration, speech, gastrointestinal motility, cardiac and vaco constrictor; reflexes are mediated (cough, gag)
cranial nuclei
134
between pons and medulla
VII and VIII
135
o Lateral medullary syndrome caused by the stroke o Frequent and violent hiccups o Contralateral loss of pain, temperature of the body, and ipsilateral loss of pain and temperature in the facial regions. Paralysis of the palate, vocal cords, vertigo
Wallenberg syndrome
136
* Inferior to the cerebral hemispheres and posterior to pons* Cerebral hemispheres – rt and lt and it is connected by vermis * Wrinkles called folia and lobes – anterior, posterior and flocculondular * Peduncles – three large fiber bundles that connects the cerebellum with spinal cord, brainstem and cerebral hemispheres * Inferior, middle, supperios
cerebellum
137
cerebellar function
motor function
138
muscle contraction in PNS; alertness, attention, memory and learning
neurotransmitter: acetylcholine
139
excitation of CNS
neurotransmitter: glutamate
140
inhibits CNS activity
neurotransmitter: GABA
141
motor control; brain reward system
neurotransmitter: dopamine
142
excited heart; fight or flight response
neurotransmitter: epinephrine
143
attention, alertness, mood
neurotransmitter: norepinephrine
144
excites/inhibits nervous system
neurotransmitter: serotonin
145
sensitizes to pain; causes inflammation
neurotransmitter: substance P