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14 Cards in this Set

  • Front
  • Back
*Neurological deficits separated in time; white matter deficits separated by space
* Women to men 2:1
* Brown glassy plaques
*Optic neuritis, CSF oligoclonal bands, motor/sensor loss of trunk, ataxia, incontinence
MS
"Asian MS"
* Plaques are more destructive than MS
* Marked spinal destruction
Delvic disease/ neuromyelitis optica
"Young MS"
* Fuliment course w/in months
Marburg form
* Headache, Lethargy, Coma
* Loss of myelin with relative sparing of axons
* Greyish discoloration around white matter vessels
* Lipid laden macrophages
* Recent viral infection
ADEM
* Symptoms similar to ADEM but more aggressive
* Disseminated necrosis of gray and white matter with hemorrhage
*Recent URI
ANEM
* Pontine lesion
* Demyelination in symmetrical pattern
* Alcoholism, liver destruction, severe electrolyte imbalance
* Rapid onset quadriplegia
Central pontine myelinolysis
Symmetrical demyelinatin in fibers of the corpus callosum
Marchiafava bignami disease
*Neurofibrillary tangles, amyloid angiopathy, neuritic plaques
*Aβ40 and Aβ42
*Memory loss/personality changes that progresses to immobile unresponsive state
* Hirano bodies, B secretase, and γ secretase
Alzheimer's Disease
* Association with defects on chromosome 21
* Increased prensenilens
* Mutation of ApoE gene on chromosome 19
Familial AD
* Accumulation of 4 repeat and 3 repeat Tau
* Atrophy of frontal and temporal lobes
* Possible Nigral loss
frontal/temporal degeneration with parkinsonism
*Frontal and temporal lobe atrophy
*Atrophy= Knife edge appearance
* Behavioral changes progressing to cognitive changes
* Cytoplasmic oval, weakly basophilic, inclusions that stain strongly with silver
* Neuronal loss in outer 3 layers of cortex
* Tangles with 3repeat Tau
Pick Disease
*trunca rigidity, nuchal dystonia, dysequilibrium
* psuedobulbar palsy
* difficulty in speech
* ocular disturbances
* mild progressive dementia
* 5th/ 6th decade
* Neuronal loss in subcortical regions
Progressive supranuclear palsy
* Balloon neurons in astrocytes, oligodendrocytes, basal ganglia, and cortical cells
* Loss of pigmentation of ceruleas and substantia
* Asymmetric motor disturbances, sensory cortical dysfunction
* Pyrmidal rigidity and cognitive decline
Corticobasal degeneration
Chorea, rigidity, postural changes
disorders of the basal ganglia