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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:...
| Autores principales: | , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2009
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2639567/ https://www.ncbi.nlm.nih.gov/pubmed/19175930 http://dx.doi.org/10.1186/1757-1626-2-94 |