Neuro 2 Flashcards

1
Q

huntingtons chorea inheritance

A

autosomal dominant

there is genetic anticipation- trinucleotide repeats increase every generation meaning onset is quicker and severity higher

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2
Q

what medication may be used in huntingtons for chorea symptoms

A

tetrabenzine

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3
Q

what tumor is myasthenia gravis associated with

A

thymoma

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4
Q

antibodies associated with myasthenia gravis

A

anti Ach receptor antibodies
MuSK antibodies
LRP4 antibodies

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5
Q

what muscles are most affected in myasthenia gravis

A

proximal muscles of the limbs
small muscles of the head and neck

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6
Q

mx of myasthenia gravis

A

pyridostigmine- cholinesterase inhibitor

immunosupression eg prenisolone or azothioprine

rituximab

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7
Q

how is a myasthenic crisis managed

A

non invasive or mechanical ventilation
IV immunoglobulins or plasmapheresis

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8
Q

lambert eaton myasthenic syndrome has autoantibodies against

A

voltage gated calcium channels on presynaptic membranes

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9
Q

features of autonomic distrubance

A

dry mouth
impotence
blurred vision
dizziness
urinary retention
ileus
heart arrythmia

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10
Q

how to differentiate myasthenia gravis from LEMs

A

LEMs muscle strength improves with use

myasthenia gravis muscle strength is worse with use

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11
Q

LEMs is associated with

A

small cell lung cancer

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12
Q

what is charcot marie tooth disease

A

an inhertied disorder causing peripheral neuropathy

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13
Q

drugs causing peripheral neuropathy

A

isoniazid
amiodarone
leflunomide
cisplatin

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14
Q

features of charcot marie tooth disease

A

peripheral neuropathy
high foot arches- pes cavus
distal muscle wasting
hyporeflexia
hypotonia

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15
Q

infections associated with GBS

A

campylobacter jejuni
cytomegalovirus
EBV

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16
Q

GBS pathophysiology

A

antibodies synthesised by B cells against the offending pathogen also fit antigens on the myelin sheath or nerve axons

17
Q

ix for GBS

A

nerve conduction studies
CSF analysis

18
Q

what does lumbar puncture show in GBS

A

raised protein with normal cell counts and glucose

19
Q

time frame of GBS

A

usually sx peak 2-4 weeks after initial infection

recovery can take months to years

20
Q

NF1 inheritance

A

autosomal dominant

21
Q

how many neurofibromas are considered significant

A

2

22
Q

sx NF1

A

neurofibromas
glioma of optic nerve
bony dysplasia- bowing
iris harmatomas
axillary freckling

23
Q

bilateral acoustic neuromas

A

NF2

24
Q

features of tuberous sclerosis

A

ash leaf spots
shagreen patch
angiofibromas (small pigmented papules across face and cheeks)
cafe au lait spots
isolated patch of white hair on head

neurological:
epilepsy
learning disability
brain tumors

25
Q

first line for chronic or frequent tension headaches

A

amitriptyline

26
Q

sinusitis mx over 10 days

A

steroid nasal spray
abx- phenoxymethylpenicillin

27
Q

what is a silent migraine

A

aura but no headache

28
Q

when are triptans used in migraine mx

A

acutely

29
Q

triptan dosing for migraines

A

take one dose as soon as sx start

if it doesnt work do not take another dose during the same attack

30
Q

triptan moa

A

5 HT receptor agonists (stimulate serotonin receptors)

31
Q

migraine prophylaxis meds

A

propanolol
topiramate
amitriptyline

32
Q

topiramate caution

A

very teratogenic- take effective contraception

33
Q

medical word for constricted pupil

A

miosis

34
Q

medial word for dilated pupil

A

mydriasis

35
Q

cluster headaches acute treatment

A

triptan
high flow oxygen

36
Q

propylaxis for cluster headache

A

verapamil