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PSYC 125 Exam 2

QuestionAnswer
"where" stream spatial location, topographical orientation, planning and coordination of movement dorsal stream
neglect, apraxia, left-right discrimination problems poor angular judgements, poor coordination of movement in space, visuoconstruction deficits, unilateral neglect, topographic disorientation dorsal stream deficits
"what" stream object recognition, matches visual shape to internal representation ventral stream
visual agnosia ventral stream deficits
failure to recognize previously familiar stimuli, modality-specific, not due to dementia/aphasia/unfamiliarity, may be limited to particular classes of stimuli agnosia
inability to recognize familiar faces prosopagnosia
inability to recognize sounds of common objects auditory sound agnosia
inability to recognize familiar people by their voices phonagnosia
inability to recognize what's placed in one hand tactile agnosia
inability to recognize what's placed in both hands (bilateral impairment) astereognosis
apperceptive agnosia and associative agnosia Lissauer's stage model types of agnosia
inability to recognize or name objects, cannot copy unrecognized objects, strong evidence for sensory-perceptual disturbance apperceptive agnosia
inability to recognize or name objects, generally can copy unrecognized objects, sensory-perceptual disturbance cannot explain defect associative agnosia
failure of perception to contact memory or language, impairment/degradation of stored representation explanations of agnosia
object agnosia, visual memory loss, superior visual field defects, achromatopsia, topographical agnosia frequent co-existing signs to agnosia
extent of damage determines presence of apperceptive defect lesion profile in prosopagnosia
discriminate age, gender, recognize emotions, recognize faces as such, match faces, show 'indirect' knowledge about faces spared abilities in prosopagnosia
identify individuals, describe the owner of the face, feel familiarity viewing faces impaired abilities in prosopagnosia
processes auditory info, tonotopic organization, Heschl's gyrus primary auditory cortex
adds meaning (language) to sound, posterior aspect of superior temporal gyrus, secondary auditory cortex wernicke's area
language expression, 3rd frontal convolution of the left interior frontal gyrus broca's area
connective fibers between wernicke's and broca's areas arcuate fasiculus
integrate visual and spatial info from occipital and parietal lobes with auditory info supramagrinal gyrus
integrates other info, plays a role in reading comprehension by matching phonemes to graphemes (sounds to words), reading and writing angular gyrus
major player; comprehension, production, meaning left hemisphere specialization in language
emotion in language, prosody (aprosodia) right hemisphere specialization in language
spontaneous speech, repetition, speech comprehension, naming, reading, writing domains of language
disturbance of language usage or comprehension, not due to motor dysfunction of mouth/vocal cords aphasia
motor dysfunction of the mouth or vocal cords dysarthria
expressive/nonfluent aphasia, primary deficit in speech production, comprehension is more or less intact broca's aphasia
receptive/fluent aphasia, primary deficit in language comprehension, speech is fluent but not in proper grammatical form wernicke's aphasia
impaired repetition, lots of hesitation, may have intact reading abilities, damage to arcuate fasiculus conduction aphasia
overall decrease in language function in multiple domains, most widespread deficits of aphasias, generally due to damage in multiple perisylvian regions global aphasia
motor and sensory transcortical aphasias
broca-like disturbed spontaneous speech, good repetition, disruption between conceptual word representations and motor speech output motor transcortical aphasia
wernicke-like impairments in word comprehension, good repetition, normal recognition of auditory words but no activation of meaning, reading and writing affected sensory transcortical aphasia
impaired single word production, mostly "everyday" nouns, repetition and comprehension intact, impaired storage or access to lexical information, damage to inferior parietal lobe or damage within perisylvian region anomia
"misspoken word" paraphasia
substituting a similar sounding word or syllable phonemic paraphasia
substituting a word with a similar context semantic paraphasia
boston diagnostic aphasia exam, boston naming test, controlled oral word association, token test neurophychological testing and language
sensory receptor - thalamic nucleus - primary cortex - secondary cortex - association cortex generic pathway of cortical organization
involves memory that occurs when information can be consciously or intentionally retrieved and stated LTM explicit memory
facts, knowledge, expertise semantic memory
personal experiences and events episodic memory
involves memory that does not require conscious or intentional retrieval LTM implicit memories
memory of motor skills and actions that have been learned previously procedural memory
acquired through classical conditioning classically conditioned responses
immediate memory, procedural memory, memory for remote events intact functions in severe amnesia
corresponds to traditional ideas of hemispheric lateralization sensory info sent to memory processing areas (hippocampus), return pathways store memories back in original cortical regions declarative memory organization
dominant lesions typically cause deficits in verbal memory left hemisphere
nondominant lesions typically lead to deficits in visual-spatial memory right hemisphere
long-term explicit semantic and episodic memories are distributed here, storage location depends on type of information cerebral cortex
critical for encoding new semantic and episodic memories, does not store long term memories, does not affect procedural memory hippocampus
important for predicting and avoiding dangerous situations, triggers hippocampus to encode details of emotional events amygdala
medial temporal lobe, diencephalon, basal forebrain declarative memory structures
center around the hippocampal formation (hippocampus proper, dentate gyrus, subiculum) medial temoral lobe structures
anterior and dorsomedial nuclei of the thalamus, mammillary bodies of the hypothalamus diencephalic structures
major declarative memory system, important for consolidation (hippocampus - mammillary bodies - anterior thalamus - cingulate gyrus) papez circuit
nucleus basalis of Meynert, substantia innominata, medial septal nucleus, nucleus of the diagonal band of Broca basal forebrain structures
implicit and explicit memory LTM
priming, conditioning, prodecural implicit
episodic and semantic explicit
cannot remember events prior to brain damage retrograde amnesia
cannot later remember events that occur after brain damage anterograde amnesia
memory storage left frontal lobe
memory retrieval right frontal lobe
knowledge of memory processes, memory contents, self-generated responses metamemory and memory monitoring
memory outside of the limbic circuitry non-declarative (implicit) memory
cerebellum, basal ganglia and motor strip brain structures of implicit memory
dementias, toxic conditions, anoxia/hypoxia, infarcts, Wernicke-Korsakoff's syndrome, head injury, seizures, transient global amnesia, psycholgenic amnesia disorders affecting memory
inability to recall events from the first 1-3 years of life infantile amnesia
encoding/storage/retrieval, immediate vs. delayed recall, recall vs. recognition, material specificity specific aspects of memory for testing
responsible for decision-making regarding personal and social matters as well as emotion processing ventromedial orbitofrontal cortex region
prefrontal area, premotor area, motor area frontal lobe anatomy
dorsolateral, orbitofrontal, medial frontal/cingulate 3 prefrontal regions
oculomotor and motor motor function of prefrontal region
dorsolateral, orbitofrontal, and anterior cingulate executive function of prefrontal region
planning, organization, selective attention, problem-solving, initiating, inhibiting, self-monitoring, abstract thinking, mental flexibility executive functions
glutamate, GABA, dopamine, acetylcholine, serotonin neurotransmitters
subserves executive function (behavioral responses, activation of remote memories, environmental independence, motor programs, verbal mediation of behavior) dorsolateral circuit function
poor organizational behavior, poor memory search strategies, environmental dependency, poor set shifting, verbal/manual dissociations dorsolateral circuit dysfunction
medial and lateral parallel circuits, personality characteristics, environmental independence, emotional continence orbitofrontal circuit function
personality changes, utilization/imitation behavior, mood disorders, OCD orbitofrontal circuit dysfunction
emotional lability, disinhibition, criminal behavior, impulsive sexual behavior, often lack awareness, anosmia, environmental dependency, pseydopsychopathic orbitofrontal syndrome
motivated behavior, drive, spontaneity, "personhood", creativity anterior cingulate functions
akinetic mutism, indifference to pain, apathy, poverty of speech, psychic emptiness, poor response inhibition anterior cingulate dysfunction
observation, questionnaires, interviews personality/behavioral assessment
sequencing, timing, and proper initiation of voluntary movements, motor planning not execution, contains mirror neurons that activate when observing movement supplementary motor cortex
disorder of motor planning, organization, and initiation injury to supplementary motor cortex
sequencing, timing, and proper initiation of voluntary movements but more in external cue rediness premotor area
emotional or motivational impetus for movement (when reward is involved) cingulate motor area
the inability to stop behaviors once they have started perseveration
failure to continue motor behavior once initiated motor impersistence
inability to execute purposeful, complex motor acts despite physical ability, comprehension, and willingness apraxia
inability to use gestures or mime tool use on command ideomotor apraxia
motor representations in which part of brain? parietal lobe
translates to movements in which part of brain? premotor cortex
primitive reflexes (grasp, sucking, utilization behavior) frontal lobe lesion signs
reduced oxygen hypoxia
absence of oxygen supply anoxia
hypoxia/anoxia, intracranial pressure if hemorrhage occurs, blood can be toxic to cerebral tissue CVA source of deficits
stable cerebral blood flow maintained by... autoregulation
reduced/blocked blood flow, increased heart rate, arterial dilation, increased oxygen extraction ratio, if none of above help cell death CVA course
insufficient blood flow to an area ischemia
sufficient disruption of blood flow to cause significant cell death infarction
small cavity caused by stroke lacune
rupture of a blood vessel, most severe form of CVA hemorrhage
temporary blockage of vessels, symptoms similar to stroke and considered a stroke warning transient ischemic attack (TIA)
thrombosis and embolism 2 primary sources of infarction
most common type, associated with atheroschlerosis thrombosis
associated with atrial fibrillation, tend to occur in younger individuals embolism
aphasia, apraxia, agraphia/dysgraphia, right hemiplegia/hemiparesis, verbal memory problems, right visual field loss, local processing deficits, depression left hemisphere deficits with CVA
visual-perceptual processing, left hemiplegia/hemiparesis, nonverbal communication, prosopagnosia, visual memory, left neglect, anosagnosia/euphoria right hemisphere deficits with CVA
rupture of blood vessel within the brain or subdural space hemorrhagic stroke
pooling of blood into the brain hematoma
pooling of blood within the cerebrum intracranial hematoma
pooling of blood into the meningial spaces subarachnoid/subdural hematoma
weakened blood vessel wall, ballooning, risk of rupture aneurysm
abnormal communication between arteries and veins, "steals" blood from other areas, high leak potential arteriovenus malformation (AVM)
cognitive decline secondary to cerebrovascular disease, definition challenges vascular dementia (VaD)
increases sick of Alzheimer's disease, cognitive symptoms neuropsychology of VaD
diffuse white matter hyperintensities, focused in the centrum semiovale and periventricular white matter Binswanger's disease
a sudden, violent, irregular movement of a limb or of the body caused by involuntary contraction of muscles convulsion
a sudden, uncontrolled electrical disturbance in the brain seizure
a neurological disorder that is a predisposition to recurrent unprovoked seizures epilepsy
structural, single/multiple lesions, medical +/- surgical treatment, responds well to certain medications partial epilepsy
whole brain, ion-channel, metabolic disease, medical treatment, can get worse with certain medications generalized epilepsy
partial, mixed, generalized 3 types epilepsy
simple and complex 2 types of partial epilepsy
generalized tonic-clonic seizure: tonic - clonic- post-ictus grand mal seizure
absence seizure, blanking out petit mal seizure
stiffening of body tonic seizure
jerking of body clonic seizure
muscle tone loss atonic seizure
brief sudden jerk myoclonic seizure
recognizes color V4 region
recognizes face FFA region / fusiform gyrus
large specificity in seizure symtoms lateral tongue biting
lack of sleep, stress, mentral cycle seizure precipitating factors
mixed seizure episode starts with focal and spreads to whole brain seizure
simple epilepsy consciousness not affected
complex epilepsy consciousness affected -- deja vu, tunnel vision, lost consciousness, etc
more intense, complex seizure seizure in association cortex
simple seizure seizure in primary cortex
complex repetitive behaviors in anterior cingulate gyrus automatism
butterfly feeling insula
fear feeling amygdala
amnesia, experiental hallucination, deja vu, jamais vu symptoms in medial temporal lobe epilepsy
mood change, attention problem, lack of confidence inter-ictal periods
genetic disposition to seizures ideopathic
Created by: 3369143883374349
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