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Summary of drugs

Pharm

QuestionAnswer
CJD rapidly progressive dementia
CJD vacuolated cortex
ALS loss of (upper) motor neurons
ALS Astrocytosis
ALS Sphincter control, sensation, intellectual function are not affected
ALS Denervation atrophy
Guillain Barre rapidly ascending paralysis that occurs over weeks
Huntington's choreiform movements, character change, or psychotic behavior
Huntington's atrophy of the caudate
frontotemporal dementia has a slow, insidious onset marked in the early stages by personality changes, then progressive loss of speech (fluent or nonfluent aphasia), apathy, and finally mutism
Guillain Barre rapidly ascending symmetric motor weakness and distal sensory impairments
ALS progressive and symmetric nature of this patient's disease
Guillain Barre absence of deeep tendon reflexes
Guillain Barre symmetric really rapid ascending progressive weakness in legs and then arms (ascending) absence of deep tendon reflexes CN involvement with ocular motility loss
Created by: ginayams
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