Generalized Lower Motor Neuron Disease Flashcards

1
Q

what can cause abnormal synaptic transmission?

A

immune mediated
toxins

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2
Q

what are the postural reactions like with generalized lower motor neuron disease?

A

normal to abnormal

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3
Q

where can the lesion be with lower motor neuron disease?

A

motor neuron
nerve root
nerve
synapse
muscle

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4
Q

which nerves can be tested for nerve conduction?

A

ulnar
radial
peroneal
tibial

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5
Q

what is the most important acquired acute generalized lower motor neuron disorder?

A

geriatric onset of laryngeal paralysis and polyneuropathy

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6
Q

what are the long peripheral nerves?

A

recurrent laryngeal nerve
sciatic nerve: tibial branch

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7
Q

what neoplasias can cause myasthenia gravis?

A

thymoma
osteosarcoma
anal sac adenocarcinoma

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8
Q

what are the early clinical signs of idiopathic distal axonopathy or geriatric onset of laryngeal paralysis and polyneuropathy?

A

voice change, clearing throat often
unspecific hind end weakness
difficulty to jump, splaying out

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9
Q

is there a causative treatment option for idiopathic distal axonopathy or geriatric onset of laryngeal paralysis and polyneuropathy?

A

no- idiopathic origin

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10
Q

what are the focal clinical signs of myasthenia gravis?

A

megaesophagus
facial, pharyngeal, laryngeal weakness

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11
Q

is repetitive nerve stimulation reliable for myasthenia gravis?

A

yes

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12
Q

what is the fulminate form of myasthenia gravis related with?

A

thymoma
high mortality

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13
Q

what can increase the survival time of myasthenia gravis?

A

immune suppressive treatment

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14
Q

what can you give to improve transmission at the synapse with myasthenia gravis?

A

pyridostigmine CRI
prednisone
pyridostigmine PO

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15
Q

what can you use to diagnose polyradiculoneuritis (coonhound paralysis)?

A

electrodiagnostics: EMG, nerve conduction

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16
Q

what can lead to primary demyelination?

A

inflammatory
toxins

17
Q

what can lead to abnormal muscle contraction?

A

myositis
dystrophy

18
Q

what are the most important acquired acute generalized lower motor neurons disorders?

A

geriatric onset of laryngeal paralysis and polyneuropathy
myasthenia gravis
idiopathic polyradiculoneuritis
botulism
tick paralysis

19
Q

what is the etiology of idiopathic distal axonopathy or geriatric onset of laryngeal paralysis and polyneuropathy?

A

disorder of long peripheral nerves
inability to transport metabolites from neurons of spinal cord to peripheral nerve ending via fast transporter system
distal axonopathy with secondary demyelination

20
Q

what is electrodiagnostic testing helpful for with idiopathic distal axonopathy or geriatric onset of laryngeal paralysis and polyneuropathy?

A

characterization of nerve dysfunction

21
Q

what antibodies are present in myasthenia gravis?

A

nicotinic receptor antibodies
striated muscle antibodies sometimes: titin or ryanodine receptor

22
Q

what happens in immune mediated receptor damage in myasthenia gravis?

A

complement
endocytosis
receptor block

23
Q

what diagnostics can be done for myasthenia gravis?

A

tensilon test
acetyl choline receptor antibody titers
repetitive nerve stimulation
radiographs/CT

24
Q

how common is muscle weakness with myasthenia gravis?

A

50%

25
Q

what can you do to neutralize antibodies in myasthenia gravis?

A

plasmapherisis, plasma exchange, multiple sessions
IgG intravenous

26
Q

what histopathologic changes occur with polyradiculoneuritis?

A

ventral nerve roots
proximal nerves
nerves distally less affected
infiltration of PMN, macrophages, later lymphocytes
axonal degeneration, demyelination

27
Q

how can you treat polyradiculoneuritis?

A

supportive care
prednisone
intravenous IgG
plasmaphoresis, plasma exchange
tumor removal if present

28
Q

what is the most important finding of generalize lower motor neuron disease?

A

decreased or absent spinal reflexes