Neurodegenerative Diseases Flashcards Preview

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Flashcards in Neurodegenerative Diseases Deck (19)
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1
Q

How are neurodegenerative diseases typically/traditionally classified?

A

• According to clinical presentation
• Alzheimers
○ Early memory and visuospatial problems
• Frontotemporal dementia
○ Early behavioral, executive and language problems
• Parkinsons
○ Tremor, rigidity, bradykinesia
• Lewy
○ Early parkinsonian features, psychosis, fluctuating consciousness
• Progressive supranuclear palsy
○ Bradykinesia, rigidity, falls, abnormal vertical eye movements
• Amyotrophic lateral sclerosis
○ Weakness and atrophy, fasciculations, and the combination of both upper and lower motor neuron signs
• Huntingtons
○ Dementia, depression, chorea
• Creutzfeldt-jakob
○ Rapidly progressive dementia with myoclunus

2
Q

What are the classic signs of CJD?

A

• Creutzfeldt-jakob

○ Rapidly progressive dementia with myoclunus

3
Q

What are the classic signs of huntington’s?

A

• Huntingtons

○ Dementia, depression, chorea

4
Q

What are the classic signs of ALS?

A

• Amyotrophic lateral sclerosis

○ Weakness and atrophy, fasciculations, and the combination of both upper and lower motor neuron signs

5
Q

what are the classic signs of progressive supranuclear palsy?

A

• Progressive supranuclear palsy

○ Bradykinesia, rigidity, falls, abnormal vertical eye movements

6
Q

what are the classic signs of lewy body disease?

A

• Lewy

○ Early parkinsonian features, psychosis, fluctuating consciousness

7
Q

what are the classic signs of parkinsons?

A

• Parkinsons

○ Tremor, rigidity, bradykinesia

8
Q

what are the classic signs of alzheimers?

A

• Alzheimers

○ Early memory and visuospatial problems

9
Q

what are the classic signs of frontotemporal dementia?

A

• Frontotemporal dementia

○ Early behavioral, executive and language problems

10
Q

Neurodegenerative diseases seem to be variations on a theme. What is the theme?

A
  • Theme - spontaneous death of neuronal populations
    • The location of the neurons determine the clinical presentation
    • Remember that neuronal location is tied to neuronal function
11
Q

What protein is implicated in frontotemporal dementia and progressive supranuclear palsy?

A
  • Abnormal tau metabolism

* Neurofibrillary tangles?

12
Q

Synuclein is a protein that when you see it you should think…?

A
  • Parkinsons

* Lewy body diseases

13
Q

Ubiquitin in the context of neurodegenerative disease makes you think…?

A
  • ALS

* Amyotrophic lateral sclerosis

14
Q

Disturbances in ach neuronal transmission makes you think:

A
  • Alzheimers and lewy body

* Though there are other pathways disturbed in each of the neuorodegen diseases

15
Q

Serotonergic dysfucntion makes you think:

A
  • Frontotemporal dementia

* Though there are other pathways disturbed in each of the neuorodegen diseases

16
Q

Disturbances in dopamine transmission makes you think:

A
  • Parkinsons and lewy body

* Though there are other pathways disturbed in each of the neuorodegen diseases

17
Q

What are the neuropathology findings of: Alzheimers

A

• Amyloid plaques and neurofibrillary tangles
• Dx requires the presence of both of these changes on pathologic examination
• Location is cortexa nd hippocampus with sparing of deeper structures
Gross - diffuse atrophy

18
Q

What are the neuropathology findings of: FTD - frontotemporal dementia

A
  • This is less of a single disease and more of a collection of pathology
    • Some have neurofibrillary tangles
    • Others have predominately ubiquitin inclusions
    • Some have tau reactive intra-neuronal inclusion
    • Some have CDP-43 deposition
    • Many have no findings at autopsy - “dementia lacking distinct histological features”
19
Q

What are the neuropathology findings of: Huntingtons

A
  • Neurodegeneration has a predilection for the caudate nucleus
    • Produces a characteristic pattern of atrophy that can be seen with neural imaging by CT or MRI

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