2003
DOI: 10.1001/archneur.60.7.1001
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Polymyositis Masquerading as Motor Neuron Disease

Abstract: Bulbar-onset polymyositis may mimic MND, particularly in the absence of inflammatory markers or elevated muscle enzyme levels. Caution should be exercised in the clinical diagnosis of bulbar dysfunction, and further investigations such as electromyography and muscle biopsy are indicated to confirm the diagnosis.

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Cited by 15 publications

(11 citation statements)
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“…Until the present study, 72.3% of our patients had a change in the diagnosis after a detailed reinvestigation. Series and cases reports [9,[11][12][13][14][15][16][17][18][19][20][21][22][23][24][25][26][27][28] corroborate our findings, showing the diagnostic difficulty and the need to redefine diagnoses in patients initially diagnosed with PM.…”
Section: Discussion
supporting
confidence: 83%