ArticleCureus2026
Progressive Bulbar Weakness in an Older Male With Suspected Double-Seronegative Myasthenia Gravis Culminating in Myasthenic Crisis: A Case Report.
Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Myasthenia gravis is a rare autoimmune disorder affecting the neuromuscular junction, causing muscle weakness that worsens with use and improves with rest. While it is typically diagnosed through antibody tests or electrophysiological testing, a smaller subset of the population is seronegative or may have inconclusive electrophysiological results. In emergent presentations, seronegative myasthenia gravis is a challenge to diagnose clinically, making it imperative to identify it early to ensure proper management and treatment. Here, we present the case of an older male with a complex medical history and suspected seronegative myasthenia gravis who through the course of his admission experienced myasthenic crisis necessitating treatment with both intravenous immunoglobulin and plasmapheresis.
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