{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,24]],"date-time":"2026-10-24T08:06:12Z","timestamp":1792829172443,"version":"4.5.0"},"reference-count":36,"publisher":"BMJ","content-domain":{"domain":["bmj.com"],"crossmark-restriction":true},"short-container-title":["Pract Neurol"],"accepted":{"date-parts":[[2026,6,17]]},"abstract":"<jats:p>\n                    Oculopharyngeal muscular dystrophy (OPMD) is a rare, late-onset disorder caused by pathogenic expansions in the\n                    <jats:italic>PABPN1<\/jats:italic>\n                    (poly(A)-binding protein nuclear 1) gene. It is characterised by progressive ptosis, dysphagia and proximal limb weakness. Due to the rarity of OPMD, patient care in general hospitals may be compromised by limited expertise, particularly during ocular, pharyngeal or gastrointestinal procedures. This can cause unnecessary complications which may be life-threatening. Here we provide a concise overview of the symptoms and signs, diagnostic investigations, counselling and symptomatic management of OPMD. We aim to contribute to the development of a tailored, multisystem approach to patient management across all care settings. We hope to improve awareness of OPMD and to improve healthcare for patients with this condition.\n                  <\/jats:p>","DOI":"10.1136\/pn-2026-005241","type":"journal-article","created":{"date-parts":[[2026,7,1]],"date-time":"2026-07-01T07:50:34Z","timestamp":1782892234000},"page":"pn-2026-005241","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":1,"title":["Oculopharyngeal muscular dystrophy: diagnosis, management and multisystem care"],"prefix":"10.1136","author":[{"ORCID":"https:\/\/orcid.org\/0009-0009-8726-7026","authenticated-orcid":false,"given":"Wesley","family":"Reintjes","sequence":"first","affiliation":[{"name":"Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Centre, Nijmegen, the Netherlands"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-9277-2643","authenticated-orcid":false,"given":"Simone","family":"Knuijt","sequence":"additional","affiliation":[{"name":"Department of Rehabilitation, Radboud University Medical Centre, Nijmegen, the Netherlands"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0009-2848-7993","authenticated-orcid":false,"given":"Fien","family":"Oelbrandt","sequence":"additional","affiliation":[{"name":"Department of Medicine, Neurology, The Ottawa Hospital, Ottawa, Ontario, Canada"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rebecca N","family":"Hastings","sequence":"additional","affiliation":[{"name":"OPMD Association, San Antonio, Texas, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Teresinha","family":"Evangelista","sequence":"additional","affiliation":[{"name":"Functional Unit of Neuromuscular Pathology, Department of Neuropathology, Myology Institute, Piti\u00e9-Salp\u00eatri\u00e8re Hospital, Assistance Publique des H\u00f4pitaux de Paris, Sorbonne University, Paris, France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-0849-9144","authenticated-orcid":false,"given":"Giorgio","family":"Tasca","sequence":"additional","affiliation":[{"name":"John Walton Muscular Dystrophy Research Centre, Faculty of Medical Sciences, Newcastle University; Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK"},{"name":"NIHR Newcastle Biomedical Research Centre (BRC), Newcastle upon Tyne, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-0187-2199","authenticated-orcid":false,"given":"Jodi","family":"Warman Chardon","sequence":"additional","affiliation":[{"name":"Department of Medicine, Neurology, The Ottawa Hospital, Ottawa, Ontario, Canada"},{"name":"Medical Genetics, CHEO, Ottawa, Ontario, Canada"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-5837-7295","authenticated-orcid":false,"given":"Nicol","family":"Voermans","sequence":"additional","affiliation":[{"name":"Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Centre, Nijmegen, the Netherlands"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"239","published-online":{"date-parts":[[2026,6,30]]},"reference":[{"key":"2026063023551002000_pn-2026-005241v1.1","doi-asserted-by":"publisher","DOI":"10.1038\/ng0298-164"},{"key":"2026063023551002000_pn-2026-005241v1.2","doi-asserted-by":"crossref","first-page":"1488","DOI":"10.1111\/ene.15252","article-title":"Clinical and genetic features of a large homogeneous cohort of oculopharyngeal muscular dystrophy patients from the Canary Islands","volume":"29","author":"Alonso-P\u00e9rez","year":"2022","journal-title":"Eur J 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Anaesthesia and neuromuscular disorders: what a neurologist needs to know. 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