Oculopharyngeal muscular dystrophy as a rare cause of dysphagia

Oculopharyngeal muscular dystrophy (OPMD) is a rare cause for late-onset dysphagia. OPMD normally follows an autosomal dominant inheritance. Herein we describe a rare case of an autosomal recessive inheritance of OPMD. An 80-year-old male presented with progressive dysphagia, frequent aspiration and...

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Detalles Bibliográficos
Autores principales: Werling, Sarah, Schrank, Bertold, Eckardt, Alexander J., Hauburger, Anja, Deschauer, Marcus, Müller, Michaela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hellenic Society of Gastroenterology 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4367226/
https://www.ncbi.nlm.nih.gov/pubmed/25831437

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4367226/
https://www.ncbi.nlm.nih.gov/pubmed/25831437

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