Week 3: Chapter 27 - Psychiatric and Related Disorders Flashcards

1
Q

What are the two major clinical categories of motor disorders?

A

Hypokinetic-Rigid Syndrome and Hyperkinetic-Dystonic Syndrome.

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2
Q

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

A

Loss of movement due to basal ganglia dysfunction.

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3
Q

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

A

Excessive or involuntary movements due to basal ganglia dysfunction.

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4
Q

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

A

George Huntington in 1872.

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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.

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6
Q

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

A

Dance-like, irregular involuntary movements.

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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.

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8
Q

What is the inheritance pattern of Huntington’s disease?

A

Autosomal dominant with complete penetrance.

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9
Q

Which brain structures show degeneration in Huntington’s disease?

A

Cortical thinning and atrophy of the basal ganglia.

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10
Q

Which neurotransmitter imbalance is associated with Huntington’s disease?

A

Dopaminergic overactivity due to GABAergic and cholinergic neuron degeneration.

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11
Q

Who described Tourette’s syndrome and when?

A

Georges Gilles de la Tourette in 1885.

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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.
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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.

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14
Q

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

A

97% show facial tics.

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15
Q

What treatments are commonly used for Tourette’s syndrome?

A

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

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16
Q

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

A

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

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17
Q

Who first described Parkinson’s disease?

A

James Parkinson in 1817.

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18
Q

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

A

A resting tremor resembling rolling a pill between fingers.

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19
Q

What is cogwheel rigidity?

A

A ratcheting resistance during passive limb movement.

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20
Q

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

A

Postural disorders, akinesia, and speech disturbances.

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21
Q

What is festination in Parkinson’s patients?

A

Uncontrolled quickening of gait steps.

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22
Q

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

A

Idiopathic, postencephalitic, and drug-induced.

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23
Q

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

A

MPTP.

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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.

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25
Q

What are common pharmacological treatments for Parkinson’s disease?

A

l-dopa, MAO inhibitors, anticholinergics, amantadine.

26
Q

What is deep brain stimulation (DBS)?

A

Surgical implantation of electrodes to reduce tremor and akinesia.

27
Q

What are the goals of pharmacological treatment in Parkinson’s?

A

Increase dopamine and suppress overactive brain regions.

28
Q

What are examples of supportive therapies for Parkinson’s?

A

Physical therapy, exercise, and psychological support.

29
Q

How does Parkinson’s disease affect cognition?

A

Slowed processing, reduced motivation, and emotional flattening.

30
Q

What are some neuropsychological test results seen in Parkinson’s patients?

A

Poor performance on working memory, verbal memory, and visuospatial tasks.

31
Q

What is the projected percentage of the population over 65 in North America and Europe by 2030?

32
Q

What percentage of people over 80 are affected by dementia?

33
Q

What is the estimated number of Americans with cognitive impairment projected for the coming decades?

A

Up to 20 million

34
Q

According to DSM-5, what distinguishes Major Neurocognitive Disorder from Mild NCD?

A

Major NCD interferes with independence; Mild NCD shows modest decline with maintained independence

35
Q

How is dementia diagnosed using standardized cognitive testing?

A

Performance 2+ SD below norms for Major NCD; 1–2 SD for Mild NCD

36
Q

What are the common causes of dementia?

A

Protein accumulations, vascular disorders, and other conditions like CTE

37
Q

What percentage of dementia cases in those over 65 is due to Alzheimer’s?

38
Q

Who first described Alzheimer’s disease and when?

A

Alois Alzheimer in 1906

39
Q

What are neuritic plaques made of?

A

Amyloid protein and degenerative neuronal fragments

40
Q

Where are paired helical filaments typically found?

A

Cortex and hippocampus

41
Q

What protein abnormality is associated with neurofibrillary tangles?

A

Tau protein

42
Q

Which cortical regions are most affected by Alzheimer’s disease?

A

Posterior parietal, inferior temporal, and entorhinal cortex

43
Q

What areas are relatively spared in Alzheimer’s disease?

A

Primary sensory and motor cortices

44
Q

What type of neuronal change is common in Alzheimer’s?

A

Neuronal shrinkage and dendritic loss

45
Q

Which neurotransmitters are reduced in Alzheimer’s?

A

ACh, noradrenaline, dopamine, serotonin, glutamate

46
Q

What distinguishes Alzheimer’s neurotransmitter profile from normal aging?

A

Pattern of multiple reductions, not just individual level

47
Q

What chromosome is the β-amyloid precursor protein gene located on?

A

Chromosome 21

48
Q

Which genes are linked to early-onset Alzheimer’s?

A

Presenilin 1 and 2

49
Q

Which gene is linked to tau protein dysfunction?

A

MAPT gene on chromosome 16

50
Q

What environmental factor has been found in higher levels in Alzheimer’s brains?

51
Q

How might the immune system contribute to Alzheimer’s?

A

Autoimmune destruction due to immune decline

52
Q

What are early symptoms of Alzheimer’s?

A

Recent memory loss and impaired attention

53
Q

How does Alzheimer’s typically progress?

A

From recent memory to remote memory and functional independence

54
Q

Which Wechsler subtests reveal Alzheimer’s impairments?

A

Digit symbol, block design, object assembly, verbal memory

55
Q

What does anomia in Alzheimer’s patients reflect?

A

Loss of semantic knowledge

56
Q

What kind of language deficits appear in Alzheimer’s?

A

Deficits in complex tasks despite simple conversation ability

57
Q

What pattern of hemisphere impairment does Alzheimer’s show?

A

Bilateral impairment

58
Q

What distinguishes Alzheimer’s from vascular dementia?

A

No sudden onset, bilateral and progressive symptoms

59
Q

What differs between early-onset and late-onset Alzheimer’s in the brain?

A

Early-onset: widespread atrophy; Late-onset: hippocampal atrophy

60
Q

Why is physical activity and social engagement important for aging individuals?

A

They help reduce dementia risk