Weakness Flashcards

(13 cards)

1
Q

What features in history help localize the cause of weakness?

A

Onset (sudden vs gradual), symmetry, proximal vs distal distribution, presence of sensory or cranial nerve symptoms, fluctuation, and associated systemic signs.

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2
Q

What is the typical pattern of weakness in upper motor neuron (UMN) lesions?

A

Spasticity, increased reflexes, upgoing plantar response (Babinski), minimal atrophy, no fasciculations.

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3
Q

What is the typical pattern of lower motor neuron (LMN) lesions?

A

Flaccid weakness, decreased reflexes, muscle atrophy, fasciculations.

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4
Q

What are common causes of sudden onset focal weakness?

A

Stroke, TIA, spinal cord compression, demyelination (e.g. MS), Todd’s paralysis (post-seizure).

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5
Q

What is the classic weakness distribution in myopathies?

A

Symmetrical, proximal muscle weakness (e.g., difficulty climbing stairs or combing hair), no sensory loss.

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6
Q

What conditions are characterized by fluctuating weakness?

A

Myasthenia gravis (ocular and bulbar involvement), Lambert-Eaton myasthenic syndrome.

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7
Q

What are red flags in a patient presenting with weakness?

A

Acute onset, respiratory compromise, bulbar symptoms, sphincter dysfunction, progressive worsening.

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8
Q

What blood tests are useful in evaluating generalized weakness?

A

Creatine kinase (CK), thyroid function, vitamin B12, electrolytes (K+, Ca2+, Mg2+), ESR/CRP, glucose.

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9
Q

What neuroimaging is indicated in new-onset or focal weakness?

A

MRI brain/spine to assess for stroke, demyelination, tumor, or spinal cord compression.

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10
Q

What test confirms the diagnosis of myasthenia gravis?

A

Anti-AChR antibodies (or MuSK antibodies), edrophonium test (rarely), and EMG with decremental response.

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11
Q

How is acute stroke managed in a patient with weakness?

A

If ischemic and within time window: thrombolysis or thrombectomy; supportive care, antiplatelets, and secondary prevention.

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12
Q

How is Guillain-Barré syndrome (GBS) managed?

A

Supportive care (monitoring respiratory function), IV immunoglobulin or plasma exchange; avoid steroids.

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13
Q

What is the treatment for myasthenia gravis?

A

Acetylcholinesterase inhibitors (e.g., pyridostigmine), immunosuppressants (steroids, azathioprine), thymectomy if indicated.

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