Disease
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Course of Illness
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Clinical Features
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Laboratory/ Radiographic Findings
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Pathological Findings
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Treatment
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Alzheimer's Disease
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Gradual onset commonly in 8th and 9th decade of life with stuttering but progressive course over 1-2 decades
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Preserved long term memory, progressive loss of short term memory, sun-downing
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Hippocampus, Temporal and parietal lobe atrophy
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Neurofibrillary Tangles, Aluminum and amyloid deposits
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acetylcholine esterase inhibotrs, NMDA recptor inhibitors with variable success to slow progression only
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Parkinson's Disease
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Gradual progression to dementia in <50% of cases
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Tremor, masked facies, shuffling gait, hallucinations, somnelence, memory improves with cuing
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Frontal lobe and substantia nigra atrophy
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substantia nigra (dopamine producing cells) atrophy and cell death
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dopamine receptor activators,dopamine replacement, transplants
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Huntington's dementia
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Progressive course over one decade starting in 4th to 6th decade of life. Strong herediatry component
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choreform (dance-like) movements, insight preserving dementia that causes paranoia, anxiety, obsessive behavior and depression
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Caudate nucleus atrophy, hereditary chromosomal aberation
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neuroleptics such as reserpine in addition to antidepressants and anxiolytics for symptomatic control
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Frontal lobe dementia (Pick's disease)
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Dis-inhibition, speech abnormalities (ecolalia, logorrhea, ...)
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Frontal lobe atrophy only
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Multi-infarct (Binswanger's dementia)
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Rapidly progressive often with a major stroke
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Progressive memory loss in a patient with multiple cardiovascular risk factors
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Lacunar infarcts in the deep white matter of the brain
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Progressive supranuclear palsy
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