NMJ Case Flashcards

(15 cards)

1
Q

cell bodies of somatic LMN are located in

A
  • cranial nerve nuclei
  • ventral horn of the spinal cord
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2
Q

where does LMN synapse with the skeletal muscle?

A

neuromuscular junction

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3
Q

Clinical Signs of Neuromuscular
Dysfunction?

A
  1. weakness
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4
Q

Acetylcholine is an important
neurotransmitter for what other types
of synapses?

A

Preganglionic sympathetic neurons

Preganglionic parasympathetic neurons

Postganglionic parasympathetic neurons

Neuromuscular junction

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5
Q

order of functional loss with spinal cord dysfunction

A
  1. proprioception lost first → loss of coordination/ataxia
  2. lack of voluntary movement (motor function)
  3. lack of superficial and deep pain → loss of somatosensory
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6
Q

Why is pain lost last?

A

Pain fibers are small and lightly myelinated → most resistant to compression

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7
Q

What anatomical factors determine order of functional loss?

A

Myelination
axon diameter
tract location within spinal cord

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8
Q

acquired myasthenia gravis?

A

immune-mediated disease where antibody binds to AChR → deficiency of AChR

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9
Q

In neuromuscular disease, are reflexes increased or decreased?

A

Decreased to absent (LMN pattern)

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10
Q

What differentiates neuromuscular weakness from spinal cord weakness?

A

NM disease → no ataxia, no proprioceptive deficits; pure weakness only

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11
Q

Do neuromuscular disorders affect proprioception?

A

No

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12
Q

Does neuromuscular disease affect mentation?

A

No

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13
Q

What examination findings support neuromuscular dysfunction?

A

Muscle atrophy or hypertrophy, decreased to absent reflexes

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14
Q

hypocalcemia and myasthenia gravis are related to

A

junctionopathy

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15
Q

hypokalemia and polymyositis are related to

A

myopathy

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