Peripheral Neuropathy Flashcards

1
Q

symptoms of large motor fibre neuropathy

A

weakness, unsteadiness, wasting
reduced power
normal sensation
absent reflexes

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2
Q

symptoms of large sensory fibre neuropathy

A

numbness, pasaesthesia, unsteadiness
normal power
vibration and joint position sense decreased
absent reflexes

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3
Q

symptoms of small fibre neuropathy

A

pain and dyesthesia (pain on touch)

normal power and reflexes pin prick and temp reduced

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4
Q

symptoms of autonomic neuropathy

A

dizziness - postural hypotension

nausea/vomiting - gastroparesis

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5
Q

foot drop and high stepping gait are signs of neuropathy in the

A

common fibular (peroneal) nerve

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6
Q

wrist drop is due to a neuropathy in

A

radial nerve

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7
Q

claw hand is due to a neuropathy in

A

ulnar nerve

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8
Q

what is pseudoathetosis

A

loss of proprioception usually seen in the hands

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9
Q

clinical signs in pseudoathetosis

A

no vibration sense in hands
cerebellar signs (but with loss of proprioception)
odd movements of hands

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10
Q

what is radiculopathy

A

damage to nerve root

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11
Q

most common area of radiculopathy

A

spine

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12
Q

clinical features of radiculopathy

A

pins and needles

loss of reflexes

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13
Q

what is plexopathy

A

problem affecting brachial or lumbar plexus

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14
Q

common cause of plexopathy

A

trauma

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15
Q

common sign of plexopathy

A

distal and proximal asymmetric weakness

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16
Q

damage to 2 or morenerves is called

A

mononeuritis multiplex

17
Q

how many nerves are affected in mononeuropathy

A

one

18
Q

how are the nerves damaged

A

axonal loss

demyelination

19
Q

acute demyelinating condition

onset is days-weeks

A

guillaine barre syndrome

20
Q

clinical manifestation of guillaine barre syndrome

A

stars with tingling limbs and pain
quadaplegia in 2 weeks
ventilation problems

21
Q

association with guillaine barre syndrome

A

post campylobacter infection

22
Q

common cause of death in guillaine barre syndrome

A

respiratory distress/failure

23
Q

treatment for guillaine barre

A

immunoglobulin infusion or plasma exchange

24
Q

most common mutation in hereditary neuropathies

A

CMT1a

25
Q

clinical features of hereditary sensory motor neuropathy type 1 (most common type)

A
champagne bottle leg sign 
hand deformities 
bones don't form properly 
pes cavus (claw foot)
26
Q

mode of inheritance of HSMN type 1

A

autosomal dominant