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Parkinson's Disease and Myasthenia Gravis Quiz
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What is the cardinal clinical feature of myasthenia gravis?
- A Distal muscle weakness with sensory loss in a glove and stocking distribution You picked ✕
- B Weakness that worsens with use and improves with rest You picked ✓
- C Muscle rigidity with resting tremor and bradykinesia You picked ✕
- D Weakness that is most severe in the morning and improves as the day progresses You picked ✕
- E Spastic weakness with hyperreflexia and an upgoing plantar response You picked ✕
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The answer is B: Weakness that worsens with use and improves with rest
Explanation
Why B is correct
See Clinical Features. Option B is correct because the cardinal feature of myasthenia gravis is fatigable weakness: muscle strength declines with repeated or sustained use and recovers with rest. The cause is a failure of transmission at the neuromuscular junction, the synapse where a motor nerve passes its signal to a muscle fibre using the chemical messenger acetylcholine. Autoantibodies (antibodies directed against the body's own tissue) have damaged the acetylcholine receptors on the muscle side, so there is little spare capacity: the first few contractions work, then the signal fails to activate enough receptors and the muscle tires. Think of a battery that runs flat with use and recharges with rest. The ocular muscles are most often affected first, causing a drooping eyelid (ptosis) and double vision (diplopia). Bulbar muscles, which control speech and swallowing, may also be involved, so a patient may slur their words or tire part-way through a meal, and the limb weakness is typically proximal and symmetrical. Sensation and deep tendon reflexes are normal, and the weakness fluctuates from hour to hour and day to day.
- Cardinal feature: Fatigable weakness that worsens with sustained use and improves with rest.
- Cause: Autoantibodies damage acetylcholine receptors at the neuromuscular junction.
- Distribution: Ocular muscles are often affected first, causing ptosis and diplopia, and bulbar muscles may be involved.
- Examination: Sensation and deep tendon reflexes are normal.
Why the other options are incorrect
- A. Distal muscle weakness with sensory loss in a glove and stocking distribution: This pattern suggests a peripheral neuropathy, in which the nerves to the hands and feet are damaged. Myasthenia gravis spares sensation and the tendon reflexes. Your answer
- C. Muscle rigidity with resting tremor and bradykinesia: Rigidity, resting tremor and slowness of movement describe Parkinson disease, a disorder of dopamine in the basal ganglia. Myasthenia gravis causes fatigable weakness, not stiffness. Your answer
- D. Weakness that is most severe in the morning and improves as the day progresses: Myasthenic weakness is not a fixed morning pattern; it increases with sustained activity and recovers with rest, so weakness that improves through the day does not describe it. Your answer
- E. Spastic weakness with hyperreflexia and an upgoing plantar response: Spasticity, brisk reflexes and an upgoing plantar response are upper motor neurone signs. In myasthenia gravis the reflexes are normal, because the problem lies at the neuromuscular junction. Your answer
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More questions from this set. Start the quiz to answer them and see each explanation.
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1
What is the primary pathological mechanism in myasthenia gravis?
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2
A 62-year-old woman with Parkinson disease is treated with co-careldopa. She reports that her tremor and rigidity improve after each dose but return before the next dose is due. Her neurologist adds entacapone. What is the primary pharmacological effect of entacapone in this context?
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