Učitavanje...
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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| Izdano u: | Ann Gastroenterol |
|---|---|
| Glavni autori: | , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Hellenic Society of Gastroenterology
2015
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4367226/ https://ncbi.nlm.nih.gov/pubmed/25831437 |
| Oznake: |
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