Neurology Flashcards

(46 cards)

1
Q

What are the diagnostic criteria for Parkinson’s disease?

A

Presence of bradykinesia with either rest tremor, rigidity or both

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2
Q

What are the three research criteria for PD?

A

Preclinical - Neurodegeneration without symptoms/signs
Prodromal - Symptoms/signs present but insufficient for diagnosis
Clinical - Diagnostic criteria met

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3
Q

What are the early symptoms/signs of PD?

A

REM behaviour disorder
Hyposmia
Constipation
Early motor impairment
Depression/anxiety
Executive dysfunction

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4
Q

What is the biggest risk factor for PD development?

A

Sibling with PD <50yo at diagnosis (LR+ 7.5)

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5
Q

What is the most protective factor against PD development?

A

Smoking (LR- 0.45)

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6
Q

What are the key histopathological findings of PD?

A

Lewy bodies (intracytoplasmic inclusions) and Lewy neurites (intra-axonal neurites) comprised of ubiquitin and alpha-synuclein

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7
Q

What is the biggest prodromal risk factor for PD?

A

RBD (LR+ 130)

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8
Q

What are the two most important genetic variations contributing to PD?

A

Glucocerebrodase (GBA) 10%
LRRK2 1-2%

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9
Q

What is the primary/concerning adverse effect of ergot-based dopamine agonists?

A

Cardiac, pulmonary and retroperitoneal fibrosis

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10
Q

Quetiapine is often used for confusion/hallucinations in PD. What important interaction needs to be considered when using quetiapine?

A

Long QT with used with domperidone (for nausea)

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11
Q

What adverse effect is more commonly seen with dopamine agonists than with levodopa?

A

Impulse control disorder

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12
Q

What adverse effect is more commonly seen with levodopa when compared to other PD treatments?

A

Dyskinesia

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13
Q

What are the features of peak-dose dyskinesia?

A

Onset 30-60 minutes post-dose, upper body chorea, patient often unaware

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14
Q

What are the features of end-dose dyskinesia?

A

Onset 3-4 hours post-dose, dystonic reactions of feet (most often), painful

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15
Q

What is the average time to onset of dementia in PD patients?

A

10 years

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16
Q

What red flags in a PD patient warrant review of the diagnosis?

A

Absence of tremor
Symmetrical signs
Falls within the first year of diagnosis
Marked speech/dysphagia
Early urinary incontinence
Early dementia within first two years

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17
Q

What are the four classic signs of PSP (Richardson’s syndrome)?

A

Early falls
Supranuclear down gaze palsy
Postural instability
Frontal dementia

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18
Q

What are the classic features of PSP-Parkinson’s?

A

Asymmetric onset
Tremor
Response to levodopa
Better prognosis

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19
Q

What is the most common presentation of corticobasal syndrome?

A

Useless, rigid, jerking arm

20
Q

What causes are there of corticobasal syndrome?

A

Corticobasal degeneration
PSP
Pick disease
Alzheimers
DLB
CJD

21
Q

What feature distinguishes the bradykinesia of PD from other causes?

22
Q

King Penguin sign on MRI is indicative of what?

23
Q

Normal midbrain with pons atrophy is indicative of what on MRI?

24
Q

What age and gender are predominantly affected by MS?

A

Females aged 20-40

25
Which five characteristic signs of MS are there?
Internuclear ophthalmoplegia Optic neuritis Acute partial myelopathy Lhermitte's symptoms Uhtoff's symptoms
26
What is the difference between relapsing remitting MS and progressive MS?
RRMS - Complete resolution of symptoms between attacks PPMS - Progressive deterioration without resolution from time of disease onset SPMS - Progressive deterioration without resolution after previous post-attack resolution
27
What level of the spinal cord are MS lesions most commonly seen?
Cervical
28
What proportion of patients with CIS and an abnormal MRI will develop MS?
70-90%
29
What CSF findings are seen with MS?
Normal CSF profile +/- mildly elevated lymphocytes Oligoclonal bands + IgG levels Normal serum oligoclonal bands
30
What relapse rates are seen with pregnant women with MS?
Increased relapse rates in first and second trimester (2-3 fold), decreased risk in third trimester
31
What are the three most important risk factors for ischaemic strokes?
Age, hypertension, atrial fibrilation
32
What are the two most important risk factors for haemorrhagic strokes?
Hypertension, cerebral amyloid angiopathy
33
What is the most common foetal abnormality seen with anti-epileptics?
Cardiac malformations
34
What is the typical age of onset for myasthenia gravis?
75 years
35
What is the test diagnostic of MG in 80% of cases?
Acetylcholinesterase antibodies
36
What is the secondary receptor to which antibodies are formed in MG?
Muscle Specific Kinase
37
Which HLA is MUSK MG associated with?
HLA DR14-DQ5
38
What is the primary treatment for MG?
Acetylcholinesterase inhibitors
39
What secondary means of treatment are there for MG?
Steroids, steroid-sparing (AZA, MTX), rituximab/eculizumab
40
What is the life-threatening complication of myasthenic crisis?
Diaphragmatic/intercostal involvement
41
What proportion of LEMS is paraneoplastic?
50% (usually SCLC)
42
What HLA class is associated with LEMS?
HLA B8-DR3
43
What antibodies are the cause of LEMS?
Anti-voltage gated calcium channel antibodies
44
What is the primary treatment of LEMS?
3-4 diaminopyridine (potassium channel blocker)
45
What is the most sensitive test for MG?
EMG
46
What is the most common pattern of peripheral neuropathy?
Distal symmetrical neuropathy