4th Year NMJ Flashcards

1
Q

what is the DN4 questionnaire used for?

A

neuropathic pain

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2
Q

management of neuropathic pain

A
amitriptyline
duloxetine
gabapentin
pregabalin
tramadol, capsaicin cream, physiotherapy and psychology
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3
Q

what should UMN facial nerve make you think?

A

stroke

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4
Q

can LMN facial nerve be managed in the community

A

yes

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5
Q

does each side of the forehead have UMN innervation?

A

yes

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6
Q

when is there forehead sparing?

A

UMN lesion of CNVII

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7
Q

what does Bells’ palsy affect?

A

LMN of CNVII

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8
Q

management of Bell’s palsy

A

prednisolone and lubricating eye drops + tape at night

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9
Q

what increases the risk of Bell’s palsy?

A

pregnancy

diabetes

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10
Q

presentation of Bell’s palsy

A
abrupt onset
unilateral face weakness
pain around ear
reduced taste
hypersensitivity to sound
unable to wrinkle forehead
dry eyes
speech difficulty
drooling
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11
Q

what causes bilateral face weakness?

A

Lyme disease

GBS

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12
Q

management of Bell’s palsy

A

steroids

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13
Q

what does bulbar palsy denote?

A

disease of the nuclei of cranial nerves IX-XII in the medulla

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14
Q

management of myasthenia crisis

A

mechanical ventilation and plasmapheresis

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15
Q

what order are muscles affected in myasthenia gravis?

A
extraocular
bulbar
face
neck
limb girdle
trunk
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16
Q

what exacerbates myasthenia gravis symptoms?

A
pregnancy
low K+
infection
temperature changes
emotion
exercise
17
Q

diagnosis of myasthenia gravis

A

examination
EMG
CT to exclude thymoma

18
Q

clinical examination points to do if myasthenia gravis suspected

A
fixed upgaze for 20 seconds (ptosis)
fixed horizontal gaze for 20s (diplopia)
sustained counting (dysarthria)
shoulder abduction 
facial weakness
19
Q

classification of myasthenia gravis

A

ocular

generalised

20
Q

management of myasthenia gravis

A
relapses= prednisolone
long-term= pyridostigmine
21
Q

management of LEMS

A

amifampridine blocks K+ channels prolonging depolarisation

22
Q

what are 50% of cases of LEMS associated with?

A

malignancy

23
Q

what is McArdle’s disease?

A

metabolic myopathy - muscle pain and weakness after exercise due to glycogen storage disorder

24
Q

causes of peripheral neuropathy

A
ABCDE
alcohol
B12 deficiency
cancer and CKD
diabetes and drugs (isoniazid, amiodarone and cisplatin)
every vasculitis
25
criteria for diagnosing GBS
Brighton criteria
26
antibody in GBS
anti-ganglioside Ab
27
what are the muscular dystrophies?
group of genetic diseases with progressive degeneration and weakness
28
examples of muscular dystrophies
Duchenne's Becker's fascioscapulohumeral muscular dystrophy
29
examples of inflammatory myopathies
inclusion body myositis polymyositis dermatomyositis
30
clinical examination muscle testing techniques
stand up with arms crossed (pelvic girdle) | raise arms above head (shoulder girdle)