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PedAM

Pediatric Disease Annotations & Medicines




Disease dysphagia
Phenotype C0270952|oculopharyngeal muscular dystrophy
Sentences 2
PubMedID- 21805106 Cricopharyngeal dilatation for the long-term treatment of dysphagia in oculopharyngeal muscular dystrophy.
PubMedID- 21602480 Introduction: oculopharyngeal muscular dystrophy (opmd) presents with progressive ptosis, dysphagia and limb girdle weakness, and is caused by expansion of a trinucleotide tandem repeat within the gene encoding poly-(a) binding protein 2.

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