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Muscular Dystrophy, Oculopharyngeal

"Muscular Dystrophy, Oculopharyngeal" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

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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.


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This graph shows the total number of publications written about "Muscular Dystrophy, Oculopharyngeal" by people in UAMS Profiles by year, and whether "Muscular Dystrophy, Oculopharyngeal" was a major or minor topic of these publications.
Bar chart showing 1 publications over 1 distinct years, with a maximum of 1 publications in 2016
To see the data from this visualization as text, click here.
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