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        <identifier>oai:figshare.com:article/34031220</identifier>
        <datestamp>2026-09-30T10:13:33Z</datestamp>
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          <dc:title>Supplemental Material for: Late-onset MuSK myasthenia gravis in a patient with poly-autoimmunity: case report and literature review</dc:title>
          <dc:creator>figshare admin karger (2628495)</dc:creator>
          <dc:creator>Russell Wong (3772600)</dc:creator>
          <dc:creator>Antonia S. Carroll (25143108)</dc:creator>
          <dc:creator>Ross Penglase (18582016)</dc:creator>
          <dc:creator>Andrew Weissberger (25143111)</dc:creator>
          <dc:creator>Stephen Tisch (9956954)</dc:creator>
          <dc:subject>Medicine</dc:subject>
          <dc:subject>Medicine</dc:subject>
          <dc:description>&lt;p dir="ltr"&gt;&lt;b&gt;Introduction&lt;/b&gt;&lt;/p&gt;&lt;p dir="ltr"&gt;Muscle-specific kinase (MuSK) myasthenia gravis (MG) is an uncommon subtype of acquired autoimmune neuromuscular junction disorder, often associated with a more severe clinical phenotype. Although MG may occasionally co-occur with other autoimmune conditions, the presence of multiple autoimmune diseases, termed poly-autoimmunity, is rare and presents significant diagnostic and therapeutic challenges.&lt;/p&gt;&lt;p dir="ltr"&gt;&lt;b&gt;Case Presentation&lt;/b&gt;&lt;/p&gt;&lt;p dir="ltr"&gt;We describe the case of a 79-year-old woman with longstanding autoimmune thyroiditis and Sjögren’s syndrome who presented with severe bulbar and axial weakness. Initially suspected to have a Sjögren’s-associated myopathy, she was later diagnosed with MuSK MG. Early empirical treatment with intravenous immunoglobulin was followed by rituximab, resulting in marked clinical improvement and sustained remission more than a year later during follow up. Concurrently, she was diagnosed with latent autoimmune diabetes in adults (LADA), raising her autoimmune burden to four counts.&lt;/p&gt;&lt;p dir="ltr"&gt;&lt;b&gt;Conclusion&lt;/b&gt;&lt;/p&gt;&lt;p dir="ltr"&gt;This case underscores the importance of clinical vigilance and multidisciplinary evaluation in patients with poly-autoimmunity and highlights the potential for personalised, mechanism-driven therapeutic approaches.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-30T10:13:33Z</dc:date>
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          <dc:identifier>10.6084/m9.figshare.34031220.v1</dc:identifier>
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