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Combined achalasia and cricopharyngeal achalasia in a patient with type 1 myotonic dystrophy: a case report
Type 1 myotonic dystrophy (MD) is a rare inherited disease which presents with skeletal muscle weakness and myotonia. Involvement of smooth muscles is also common and mainly manifests in the gastrointestinal tract. We report a case of type 1 MD who presented with dysphagia and was found to have uniq...
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| Publicado en: | Gastroenterol Hepatol Bed Bench |
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| Autores principales: | , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Shaheed Beheshti University of Medical Sciences
2020
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7149813/ https://ncbi.nlm.nih.gov/pubmed/32308942 |
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