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Oculopharyngeal muscular dystrophy as a rare differential diagnosis for unexplained dysphagia: a case report
INTRODUCTION: We wish to report on a rare cause of dysphagia; oculopharyngeal muscular dystrophy (OPMD). It is a late adult onset autosomal dominant form of muscular dystrophy that constitutes as a rare diagnosis for any place outside of Canada and first case in southern Germany. CASE PRESENTATION:...
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| Asıl Yazarlar: | , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BioMed Central
2009
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2639567/ https://ncbi.nlm.nih.gov/pubmed/19175930 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1757-1626-2-94 |
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