G.P.8
Oculopharyngodistal myopathy (OPDM) is a rare, adult-onset, slowly progressive hereditary vacuolar myopathy in which the weakness and atrophy affect oculofacial, pharyngeal and distal skeletal muscles. The underlying genetic defect is yet unknown. Swallowing difficulties and hoarseness due to oropha...
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Published in: | Neuromuscular disorders : NMD Vol. 24; no. 9; p. 796 |
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Main Authors: | , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
01-10-2014
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Subjects: | |
Online Access: | Get full text |
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