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Brain area associated w/ tactile agnosia
Parietal lobe
Brain area damaged w/ VISUAL agnosia
Bilateral occipital lobe or posterior parietal lobe
Brain area damaged w/ Auditory Verbal agnosia
Bilateral temporal lobe lesions that isolate Wernicke’s area
Auditory Verbal agnosia - what is intact what is not?
Damaged - spoken words
Intact - 1. peripheral hearing, 2. recognition of nonverbal sounds, 3. recognition of printed words, and 4. (relatively) normal verbal expression and reading
Auditory agnosia - what is impaired what is intact?
Impaired: understanding of the meaning of auditory stimuli, and matching objects with their sound
intact: peripheral hearing, visual recognition of objects
What brain area is damaged in Auditory Agnosia?
Bilateral damage to the auditory association area
Types of agnosia
Auditory
Auditory Verbal
Visual
Tactile
BONUS: Prosopagnosia
3 Main Sub-types of Aphasia?
Fluent
Non-Fluent
Sub-cortical
6 Main treatment areas of aphasia?
Auditory comprehension
Verbal expression (naming)
Verbal expression (expanded utterances)
Alexia (reading)
Agraphia (writing)
Agnosia
Alexia (definition) + pure alexia (definition and brain area)
Broad definition: a loss of previously acquired reading skills due to brain damage
Pure definition: reading problem when wiring and other language skills are intact. Lesion in inferior occipitotemporal region
Agraphia (definition plus brain area damaged)
Def: loss of normally acquired writing skills
Brain damage: lesions in the medial frontal gyrus also called Exner’s writing area
Dementia prevalence rates + rates of early onset vs late onset Alzheimer’s Dementia
As high as 25% in ppl over 65 years old. After the age of 65, it doubles every 5 years
Only 6% of AD is Early Onset. Rest is in 70’s or 80’s
Areas of Cognition affected by dementia
Complex attention
Executive function
Learning
Memory
Language
Perceptual-motor
Social cognition
Alzheimer’s Dementia - types of neuropathology that cause it
Neurofibrillary tangles (literally tangled, twisted, thickened structures in nerve cells, dendeites and axons)
Neuritic plaques aka amyloid plaques (abnormal deposits of amyloid protein - cortical and subcortical tissue degeneration especially the hippocampus and cerebral cortex)
Granulovacuolar degeneration (cavities of granular debris in hippocampus)
Neuronal loss or general neuronal atrophy - brain shrinkage
Neuro-chemical changes (depleted neurochemicals that help transmit messages across the brain)
Symptoms of EARLY STAGE DAT (dementia of Alzheimer’s type)
Subtle memory problems
Difficulty with new leaning and visuospatial problems
Behavior changes - self neglect and avoiding routines
Indifference, irritability, depression
Slight disorientation in new surroundings
Subtle language changes
** motor functions are normal
Symptoms of MID-LATE STAGE DAT
Severe problems recalling remote and recent events
Visuospatial problems
Intellectual deterioration
Hyperactivity, restlessness, wandering, Agitation
lack of affect, tact and judgement, loss of initiative, indifference
Problems with math
Can’t manage daily routines
Profound disorientation to place, time, and person
Paranoid delusions and hallucinations
Aggressive disruptive
Inappropriate humor/laughter
Sun downing (worse at night)
Latest stage: seizures, myoclonic jerks, incontinence, dysphagia, physical deterioration, severe decline in motor function
LANGUAGE symptoms of DAT (plus aside about the FINAL stages)
General word finding
Naming
Verbal and literal paraphasias
Circumlocution
Difficulty comprehending abstract meanings
Hard to do a picture description, generate a list of words
Echolalia, palilalia, logoclonia
Empty speech, jargon, hyper fluency, inappropriate
Incoherent, slurred, rapid speech
Reading and writing difficulties
Inattention to social conventions, initiating and maintaining conversation
FINAL FINAL: no meaningful speech, mutism, complete disorientation to time, place, AND self
Echoalia vs Palilalia vs. Logoclonia
Echoalia - repeating other people’s speech
Palilalia - repeating your own utterances
Logoclonia - repeating the final syllable of words
Pick’s Disease (aka FTD)
(Onset, neuro damage/disease, impairments)
Type of front-temporal dementia. Fairly common. Earlier onset (40-60 yrs.)
Caused by degeneration of left and right frontal lobe, temporal lobes, or both.
Presence of a Pick bodies or Pick cells (atrophied, gliosed, swollen brain cells)
results in behavior changes (especially in right atrophy) and language loss (left sided atrophy)
Behavior changes: uninhibited and inappropriate, compulsive, emotional disturbances, impaired judgement/reasoning/insight
Language changes: impaired comprehension, word finding, paraphasia, circumlocution, difficulty defining words/remembering category words, limited spontaneous, Echolalia
PPA (primary progressive aphasia)
Progressive neuropathology (unlike sudden onsent of symptoms with CVA - stroke), language impairment and relatively intact cognitive skills until 2 years post onset
3 TYPES (tho not everyone fits neatly)
****mneumonic: SNL****
Nonfluent variant (NfvPPA): limited to the left perisylvian language area including Broca’s, sometimes ppl also show Parkinsonian features, 2nd most common variant, slow progression, relatively intact cognition and memory/ADL’s /job for 2 years, behavior changes within 2 years. Language is earliest signs: Anomia, word-finding, paraphasias, apraxia, reduced fluency, slow rate, agrammatism, impaired repetition, mimics Broca’s, prosody issues
Semantic Variant (SvPPA): more rare variant, temporal lobe atrophies first then frontal lobe. Behavior changes in later stages. Language: progressive loss of word meaning, anomia, semantic paraphasias, intact fluency and repetition skills, intact phonological and motor skills (no apraxia), logorrhea, impaired turn-taking, short phrases/eventual mutism, Visual agnosia + prosopagnosia (right temporal lobe)
Logopenic Variant (lvPPA): ~controversial~ left posterior superior temporal and middle temporal gyri and the inferior parietal lobe, most common variant (35%), behavior changes, language: only moderate naming difficulties in earlier stages, slow speech, word-finding pauses like non-fluent but unlike non-fluent NO agrammatism, motor issues, telegraphic speech or prosody issues, severely impaired repetition, impaired comprehension
Parkinson’s Disease (dementia + other symptoms)
Big symptoms: hypokinesia, tremor, and muscular rigidity. Only 35-55% of pt’s have dementia. Areas affected - basal ganglia, brainstem, lewy bodies in the substantia nigra, frontal lobe atrophy.
Other symptoms:
Neuro - slow movements (bradykinesia), tremor, muscular rigidity, blunted affect, festination gate, freezing, cogwheel rigidity, swallowing disorders
Speech Symptoms - reduced volume, mono pitch, monoloudness, pausing speech, slow/fast/festinating speech rate, dysarthric speech, memory problems/abstract reasoning/problem solving, naming and language comprehension, micrographia
Athetosis
Involuntary writhing
Example disorder - Creutzfeldt-Jakob disease
Infectious Dementias (2)
AIDS-related or HIV-encephalopathy: slow onset and rapid progression, gait, tremor, seizures, ataxia, rigidity, weakness, paralysis, poor memory/concentration, apathy/psychiatric symptoms
Creutzfeldt-Jakob disease: infectious agent called a PRION causes widespread spongiform state in the brain. Motor symptoms like cerebellar ataxia, memory, reasoning, sleep issues, psychiatric issues
Both = final stage of mutism