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
Q

criteria for diagnosing GBS

A

Brighton criteria

26
Q

antibody in GBS

A

anti-ganglioside Ab

27
Q

what are the muscular dystrophies?

A

group of genetic diseases with progressive degeneration and weakness

28
Q

examples of muscular dystrophies

A

Duchenne’s
Becker’s
fascioscapulohumeral muscular dystrophy

29
Q

examples of inflammatory myopathies

A

inclusion body myositis
polymyositis
dermatomyositis

30
Q

clinical examination muscle testing techniques

A

stand up with arms crossed (pelvic girdle)

raise arms above head (shoulder girdle)