Neuro - Chronic Disorders Flashcards

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1
Q

what triad of symptoms makes up parkinsonism?

A

rigidity
tremor
bradykinesia

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2
Q

risk factors for parkinson’s?

A

age
FHx
head injury
drugs

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3
Q

what drugs can cause parkinsonism?

A
typical antipsychotics (older)
legal highs
anti emetics (dopamine antagonist e.g prochloperazine)
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4
Q

features of parkinson’s?

A
pill rolling tremor at rest
cog wheel
shuffling gait 
postural instability
lack of arm swing 
hypomimia
reduced blink rate
micrographia
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5
Q

systemic features of parkinson’s?

A
anosmia
REM sleep disorders
retention/constipation
depression
hallucination 
postural hypotension
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6
Q

how can drug induced parkinson’s present?

A

symmetrical
tardive dyskinesia
akathasia
orolingual dyskinesia

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7
Q

pathology or parkinson’s?

A

loss of dopaminergic neurons in the substantia nigra of the basal ganglia

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8
Q

Ix for parkinson’s?

A
clinical (improves with L dopa use)
MRI
DAT scan (reduced uptake in basal ganglia)
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9
Q

Tx for parkinson’s?

A

L dopa + COMT inhibitor (e.g carbidopa)

dopamine agonist e.g pramipexole, bromocriptine

MAO B inhibitor e.g selegeline

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10
Q

complications of dopaminergic therapy?

A

dyskinesias (‘freezes’ as drug stops working then excess movement)

compulsive behaviour
nausea
hypotension
arrythmias

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11
Q

is smoking good or bad for parkinson’s?

A

good

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12
Q

what are parkinson’s plus syndromes?

A

have the core features of parkinsonism but can be distinguished

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13
Q

how to distinguish multi system atrophy from parkinson’s?

A

impotence

urinary retention/incontinence

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14
Q

how to distinguish progressive supranuclear palsy from parkinson’s?

A

difficulty moving eyes vertically

loss of balance

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15
Q

how to distinguish corticobasal degen from parkinson’s?

A

movement disorder is worse

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16
Q

what are LMN signs?

A

weakness
fasciculations
atrophy
hyporeflexia

17
Q

what features MND NOT have?

A

sensory loss
sphincter disturbance
eye movement changes

18
Q

most common type of MND? what signs are there?

A

ALS

UMN + LMN

19
Q

what does progressive bulbar palsy affect?

A

CN IX-XII

progresses to ALS

20
Q

what does progressive muscular atrophy affect?

A

LMN
distal then proximal muscles
best prognosis

21
Q

what does primary lateral sclerosis affect?

A

UMN

22
Q

in MND, where can there be a loss of neurone?

A

pre central gyrus
motor CNs
anterior horn cells

23
Q

Tx for MND?

A

MDT approach
riluzone
baclofen
antidepressants

24
Q

what happens in myasthenia gravis?

A

antibodes to acetyl choline receptors attack

destroy post synaptic membrane of the NMJ

reduced muscle fibre action potentials

25
Q

features of myasthenia gravis?

A
muscle weakness worse at end of day
proximal weakness
ptosis
diplopia
dysphagia
dysarthria
facial weakness
SOB
normal reflexes
26
Q

Ix for myasthenia gravis?

A

serum AChR Abs
MuSK Abs
pulmonary function tests (FVC)

27
Q

Tx for myasthenia gravis?

A

pyridogstimine
pred
IV Igs/plasma in crisis

28
Q

in a myasthenia gravis crisis, what changes can occur on PFTs?

A

low FVC

low NIF

29
Q

what are those with myasthenia gravis at higher risk of developing?

A

thymoma