Year 2016 / Volume 108 / Number 12
Letter to the Editor
Utility of surgical myotomy in the dysphagia due to oculopharyngeal dystrophy

843-844

DOI: 10.17235/reed.2016.4266/2016

M.ª Asunción Acosta Mérida, Joaquín Marchena Gómez, Josefa M.ª Afonso Déniz,

Abstract
Oculopharyngeal muscular dystrophy (OPMD), is a rare hereditary myopathy that affects mainly the levator palpebrae and the constrictor pharyngeal muscles, being able to cause severe dysphagia. It can be treated effectively by surgical cricopharyngeal myotomy, as in the case presented below.
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References
1. Clavé P, Terré R, de Kraa M et al. Approaching oropharyngeal dysphagia. Rev Esp Enferm Dig 2004; 96:119-31
2. Brais B, Bouchard JP, Xie YG et al. Short GCG expansions in the PAPB2 gene cause oculopharyngeal muscular dystrophy. Nat Genet 1998; 18:164-167
3. Gómez-Torres A, Abrante-Jiménez A, Rivas-Infante E et al. Miotomía del cricofaríngeo en el tratamiento de la distrofia muscular oculofaríngea. Acta Otorrinolaringol Esp 2012; 63:465-469
4. Kos MP, David EF, Klinkenberg-Knol EC et al. Long-Term Results of External Upper Esophageal Sphincter Myotomy for Oropharyngeal Dysphagia. Dysphagia 2010; 25:169–176
5. Coiffier L, Périé S, Laforêt P et al. Long-term results of cricopharyngeal myotomy in oculopharyngeal muscular dystrophy. Otolaryngol Head Neck Surg 2006; 135:218-222
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Acosta Mérida M, Marchena Gómez J, Afonso Déniz J. Utility of surgical myotomy in the dysphagia due to oculopharyngeal dystrophy. 4266/2016


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Publication history

Received: 11/02/2016

Accepted: 13/04/2016

Online First: 04/11/2016

Published: 30/11/2016

Article revision time: 47 days

Article Online First time: 267 days

Article editing time: 293 days


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