 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.
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.
| Descriptor ID |
D039141
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| MeSH Number(s) |
C05.651.534.500.450 C10.668.491.175.500.450 C16.320.577.450
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| Concept/Terms |
Muscular Dystrophy, Oculopharyngeal- Muscular Dystrophy, Oculopharyngeal
- Dystrophies, Oculopharyngeal Muscular
- Dystrophy, Oculopharyngeal Muscular
- Muscular Dystrophies, Oculopharyngeal
- Oculopharyngeal Muscular Dystrophies
- Oculopharyngeal Dystrophy
- Progressive Muscular Dystrophy, Oculopharyngeal Type
- Oculopharyngeal Muscular Dystrophy
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Below are MeSH descriptors whose meaning is more general than "Muscular Dystrophy, Oculopharyngeal".
Below are MeSH descriptors whose meaning is more specific than "Muscular Dystrophy, Oculopharyngeal".
This graph shows the total number of publications written about "Muscular Dystrophy, Oculopharyngeal" by people in this website by year, and whether "Muscular Dystrophy, Oculopharyngeal" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2016 | 0 | 1 | 1 |
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Below are the most recent publications written about "Muscular Dystrophy, Oculopharyngeal" by people in Profiles.
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Bennett B, Helbling D, Meng H, Jarzembowski J, Geurts AM, Friederich MW, Van Hove JLK, Lawlor MW, Dimmock DP. Potentially diagnostic electron paramagnetic resonance spectra elucidate the underlying mechanism of mitochondrial dysfunction in the deoxyguanosine kinase deficient rat model of a genetic mitochondrial DNA depletion syndrome. Free Radic Biol Med. 2016 Mar; 92:141-151.
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