Week 3: Chapter 27 - Psychiatric and Related Disorders Flashcards

(60 cards)

1
Q

What are the two major clinical categories of motor disorders?

A

Hypokinetic-Rigid Syndrome and Hyperkinetic-Dystonic Syndrome.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What characterizes hypokinetic-rigid syndromes like Parkinson’s disease?

A

Loss of movement due to basal ganglia dysfunction.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What defines hyperkinetic-dystonic syndromes such as Huntington’s and Tourette’s?

A

Excessive or involuntary movements due to basal ganglia dysfunction.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Who first described Huntington’s disease and in what year?

A

George Huntington in 1872.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What are the typical age of onset and average duration of Huntington’s disease?

A

Typically begins between ages 30 and 50; average survival is about 12 years.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are choreas in the context of Huntington’s disease?

A

Dance-like, irregular involuntary movements.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What types of emotional and cognitive symptoms are seen in Huntington’s disease?

A

Memory issues, slowed processing, depression, mania, and psychotic episodes.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is the inheritance pattern of Huntington’s disease?

A

Autosomal dominant with complete penetrance.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Which brain structures show degeneration in Huntington’s disease?

A

Cortical thinning and atrophy of the basal ganglia.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Which neurotransmitter imbalance is associated with Huntington’s disease?

A

Dopaminergic overactivity due to GABAergic and cholinergic neuron degeneration.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Who described Tourette’s syndrome and when?

A

Georges Gilles de la Tourette in 1885.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What are the three stages of symptom development in Tourette’s syndrome?

A
  1. Motor tics
  2. Inarticulate vocalizations
  3. Vocal tics like echolalia and coprolalia.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is coprolalia and how is it related to Tourette’s syndrome?

A

Involuntary use of obscene language seen in some Tourette’s patients.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What percentage of Tourette’s patients exhibit motor tics in the face?

A

97% show facial tics.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What treatments are commonly used for Tourette’s syndrome?

A

Antidopaminergic drugs (e.g., haloperidol) and clonidine.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What cognitive deficits are commonly found in Tourette’s patients?

A

Impairments in visuospatial tasks like the Rey Complex-Figure Test.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Who first described Parkinson’s disease?

A

James Parkinson in 1817.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What is the ‘pill-rolling’ tremor in Parkinson’s disease?

A

A resting tremor resembling rolling a pill between fingers.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

What is cogwheel rigidity?

A

A ratcheting resistance during passive limb movement.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

What are examples of negative symptoms in Parkinson’s disease?

A

Postural disorders, akinesia, and speech disturbances.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

What is festination in Parkinson’s patients?

A

Uncontrolled quickening of gait steps.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

What are the three major types of Parkinson’s disease?

A

Idiopathic, postencephalitic, and drug-induced.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

What toxin in synthetic heroin can cause Parkinson-like symptoms?

A

MPTP.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

What is the role of the substantia nigra in Parkinson’s disease?

A

Produces dopamine and sends projections to the cortex and basal ganglia.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
What are common pharmacological treatments for Parkinson’s disease?
l-dopa, MAO inhibitors, anticholinergics, amantadine.
26
What is deep brain stimulation (DBS)?
Surgical implantation of electrodes to reduce tremor and akinesia.
27
What are the goals of pharmacological treatment in Parkinson’s?
Increase dopamine and suppress overactive brain regions.
28
What are examples of supportive therapies for Parkinson’s?
Physical therapy, exercise, and psychological support.
29
How does Parkinson’s disease affect cognition?
Slowed processing, reduced motivation, and emotional flattening.
30
What are some neuropsychological test results seen in Parkinson’s patients?
Poor performance on working memory, verbal memory, and visuospatial tasks.
31
What is the projected percentage of the population over 65 in North America and Europe by 2030?
0.2
32
What percentage of people over 80 are affected by dementia?
25–50%
33
What is the estimated number of Americans with cognitive impairment projected for the coming decades?
Up to 20 million
34
According to DSM-5, what distinguishes Major Neurocognitive Disorder from Mild NCD?
Major NCD interferes with independence; Mild NCD shows modest decline with maintained independence
35
How is dementia diagnosed using standardized cognitive testing?
Performance 2+ SD below norms for Major NCD; 1–2 SD for Mild NCD
36
What are the common causes of dementia?
Protein accumulations, vascular disorders, and other conditions like CTE
37
What percentage of dementia cases in those over 65 is due to Alzheimer’s?
~65%
38
Who first described Alzheimer’s disease and when?
Alois Alzheimer in 1906
39
What are neuritic plaques made of?
Amyloid protein and degenerative neuronal fragments
40
Where are paired helical filaments typically found?
Cortex and hippocampus
41
What protein abnormality is associated with neurofibrillary tangles?
Tau protein
42
Which cortical regions are most affected by Alzheimer’s disease?
Posterior parietal, inferior temporal, and entorhinal cortex
43
What areas are relatively spared in Alzheimer’s disease?
Primary sensory and motor cortices
44
What type of neuronal change is common in Alzheimer’s?
Neuronal shrinkage and dendritic loss
45
Which neurotransmitters are reduced in Alzheimer’s?
ACh, noradrenaline, dopamine, serotonin, glutamate
46
What distinguishes Alzheimer’s neurotransmitter profile from normal aging?
Pattern of multiple reductions, not just individual level
47
What chromosome is the β-amyloid precursor protein gene located on?
Chromosome 21
48
Which genes are linked to early-onset Alzheimer’s?
Presenilin 1 and 2
49
Which gene is linked to tau protein dysfunction?
MAPT gene on chromosome 16
50
What environmental factor has been found in higher levels in Alzheimer’s brains?
Aluminum
51
How might the immune system contribute to Alzheimer’s?
Autoimmune destruction due to immune decline
52
What are early symptoms of Alzheimer’s?
Recent memory loss and impaired attention
53
How does Alzheimer’s typically progress?
From recent memory to remote memory and functional independence
54
Which Wechsler subtests reveal Alzheimer’s impairments?
Digit symbol, block design, object assembly, verbal memory
55
What does anomia in Alzheimer’s patients reflect?
Loss of semantic knowledge
56
What kind of language deficits appear in Alzheimer’s?
Deficits in complex tasks despite simple conversation ability
57
What pattern of hemisphere impairment does Alzheimer’s show?
Bilateral impairment
58
What distinguishes Alzheimer’s from vascular dementia?
No sudden onset, bilateral and progressive symptoms
59
What differs between early-onset and late-onset Alzheimer’s in the brain?
Early-onset: widespread atrophy; Late-onset: hippocampal atrophy
60
Why is physical activity and social engagement important for aging individuals?
They help reduce dementia risk