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Muscular Dystrophy, Oculopharyngeal MeSH Descriptor Data 2026
An autosomal dominant hereditary disease that presents in late in life and is characterized by DYSPHAGIA and progressive ptosis of the eyelids. Mutations in the gene for POLY(A)-BINDING PROTEIN II have been associated with oculopharyngeal muscular dystrophy.
Entry Term(s)
Oculopharyngeal Dystrophy
Oculopharyngeal Muscular Dystrophy
Progressive Muscular Dystrophy, Oculopharyngeal Type
An autosomal dominant hereditary disease that presents in late in life and is characterized by DYSPHAGIA and progressive ptosis of the eyelids. Mutations in the gene for POLY(A)-BINDING PROTEIN II have been associated with oculopharyngeal muscular dystrophy.