The key finding in myotonic dystrophy in a newborn is dysfunctional muscle relaxation. Which description best matches this?

Study for the NBME Form 13 Test with our comprehensive quiz collection, featuring flashcards and multiple-choice questions to ensure your readiness. Enhance your knowledge with detailed explanations for each question.

Multiple Choice

The key finding in myotonic dystrophy in a newborn is dysfunctional muscle relaxation. Which description best matches this?

Explanation:
The main idea being tested is myotonia—the delayed relaxation of skeletal muscle after contraction. In myotonic dystrophy, the muscle membrane remains hyperexcitable after a burst of activity, so the muscle takes longer to return to its resting length. That’s why the best description is prolonged muscle relaxation: after a contraction or quick stretch, the muscle does not promptly relax. Hyperreflexia isn’t typical here because this is a myopathy with normal or decreased reflexes rather than an upper motor neuron–type hyperreflexia. Fasciculations are random twitches from motor unit instability and aren’t the hallmark of myotonic dystrophy.

The main idea being tested is myotonia—the delayed relaxation of skeletal muscle after contraction. In myotonic dystrophy, the muscle membrane remains hyperexcitable after a burst of activity, so the muscle takes longer to return to its resting length. That’s why the best description is prolonged muscle relaxation: after a contraction or quick stretch, the muscle does not promptly relax.

Hyperreflexia isn’t typical here because this is a myopathy with normal or decreased reflexes rather than an upper motor neuron–type hyperreflexia. Fasciculations are random twitches from motor unit instability and aren’t the hallmark of myotonic dystrophy.

Subscribe

Get the latest from Passetra

You can unsubscribe at any time. Read our privacy policy