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We report a patient with atypical OPMD who also had acetylcholine receptor antibody-mediated myasthenia gravis. This report raises awareness of the diagnostic and treatment implications of the association of myasthenia gravis with genetic myopathies.<\/jats:p>","DOI":"10.1136\/practneurol-2022-003429","type":"journal-article","created":{"date-parts":[[2022,5,13]],"date-time":"2022-05-13T06:14:19Z","timestamp":1652422459000},"page":"413-414","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":7,"title":["Oculopharyngeal muscular dystrophy coexisting with myasthenia gravis"],"prefix":"10.1136","volume":"22","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-8388-4010","authenticated-orcid":false,"given":"Anca Loredana","family":"Alungulese","sequence":"first","affiliation":[{"name":"Department of Neurology, Principe de Asturias University Hospital, Madrid, Spain"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Miguel Angel","family":"Garc\u00eda Soldevilla","sequence":"additional","affiliation":[{"name":"Department of 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