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:...

Descripción completa

Detalles Bibliográficos
Autores principales: Bumm, Klaus, Zenker, Martin, Bozzato, Alessandro
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Case Report
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

Internet

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

Ejemplares similares