<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" article-type="Case Report" dtd-version="1.0"><front><journal-meta><journal-id journal-id-type="pmc">iarjmcr</journal-id><journal-id journal-id-type="pubmed">IARJMCR</journal-id><journal-id journal-id-type="publisher">IARJMCR</journal-id><issn>2709-3220</issn></journal-meta><article-meta><article-id pub-id-type="doi">https://doi.org/10.47310/iarjmcr.2022.v03i02.016</article-id><title-group><article-title>Rare Case of Myasthenia Gravis with Necrotizing Myopathy</article-title></title-group><contrib-group><contrib contrib-type="author"><name><given-names>Ahmed</given-names><surname>Harazeen</surname></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><given-names>Rasha</given-names><surname>Alfattal</surname></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><given-names>Neeharika</given-names><surname>Thottempudi</surname></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><given-names>Chilvana</given-names><surname>Patel</surname></name></contrib></contrib-group><aff-id id="aff-a" /><abstract>Idiopathic Necrotizing Autoimmune Myopathy (INAM) is a rare form of inflammatory myopathy characterized by necrosis and regeneration of myocytes without significant inflammation. Concurrence of inflammatory myopathy and Myasthenia Gravis (MG) is very rare. Here we present a rare case of INAM and MG after thymectomy.</abstract></article-meta></front><body /><back /></article>