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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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Detalles Bibliográficos
Autores principales: Ghazaleh, Sami, Nehme, Christian, Khader, Yasmin, Hasan, Syed, Nawras, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shaheed Beheshti University of Medical Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7149813/
https://www.ncbi.nlm.nih.gov/pubmed/32308942