Disease #05752 (OPML (myopathy, oculopharyngeal, with leukoencephalopathy (OPML)))

Official abbreviation OPML
Name myopathy, oculopharyngeal, with leukoencephalopathy (OPML)
OMIM ID -
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Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 0 genes -
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Date created 2020-05-19 08:39:23 +02:00 (CEST)
Date last edited N/A


Individuals

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00301598 FamF5305 PubMed: Ishiura 2019 4-generation family, 7 affected (4F, 3M) - - Japan - - - - - OPML leukoencephalopathy, MRI brain increased DWI signal intensity frontal corticomedullary junctions, ptosis, restricted eye movements, dysphagia, dysarthria, diffuse limb muscle weakness with nonspecific myopathic changes in muscle biopsy specimens; severe gastrointestinal dysmotility (III3/6), respiratory failure (III3/6); mild ataxia (III3), bladder disturbances (III3), dilated cardiomyopathy (III3); hand tremor (III5) NUTM2B-AS1 NUTM2B-AS1 1 7 Johan den Dunnen
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