oculopharyngeal muscular dystrophy
Oculopharyngeal muscular dystrophy (OPMD) is an adult-onset progressive myopathy characterized by progressive eyelid ptosis, dysphagia, dysarthria and proximal limb weakness
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oculopharyngeal muscular dystrophy
Summary
oculopharyngeal muscular dystrophy is a rare disease[1]. It draws 28 Wikipedia views per month (rare_disease category, ranking #216 of 627).[2]
Key Facts
- oculopharyngeal muscular dystrophy's instance of is recorded as rare disease[3].
- oculopharyngeal muscular dystrophy's instance of is recorded as class of disease[4].
- oculopharyngeal muscular dystrophy is a type of myopathy of extraocular muscle[5].
- oculopharyngeal muscular dystrophy is a type of muscular dystrophy[6].
- oculopharyngeal muscular dystrophy is a type of progressive muscular dystrophy[7].
- oculopharyngeal muscular dystrophy is a type of ptosis[8].
- oculopharyngeal muscular dystrophy's symptoms and signs is recorded as ptosis[9].
- oculopharyngeal muscular dystrophy's symptoms and signs is recorded as dysphagia[10].
- oculopharyngeal muscular dystrophy's symptoms and signs is recorded as dysarthria[11].
- oculopharyngeal muscular dystrophy's has cause is recorded as trinucleotide repeat expansion[12].
- oculopharyngeal muscular dystrophy's medical examination is recorded as genetic testing[13].
- oculopharyngeal muscular dystrophy's medical examination is recorded as muscle biopsy[14].
- oculopharyngeal muscular dystrophy's possible treatment is recorded as speech therapy[15].
- oculopharyngeal muscular dystrophy's possible treatment is recorded as dietary supplement[16].
- oculopharyngeal muscular dystrophy's prevalence is recorded as {'amount': '+0.000001'}[17].
- oculopharyngeal muscular dystrophy's NCI Thesaurus ID is recorded as C84942[18].
- oculopharyngeal muscular dystrophy's health specialty is recorded as neurology[19].
- oculopharyngeal muscular dystrophy's genetic association is recorded as PABPN1[20].
- oculopharyngeal muscular dystrophy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_11719[21].
- oculopharyngeal muscular dystrophy's exact match is recorded as http://identifiers.org/doid/DOID:11719[22].
- oculopharyngeal muscular dystrophy's on focus list of Wikimedia project is recorded as WikiProject Medicine[23].
Why It Matters
oculopharyngeal muscular dystrophy draws 28 Wikipedia views per month (rare_disease category, ranking #216 of 627).[2] It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[24] It is known by 11 alternative names across languages and contexts.[25]