Clinical and Muscle Imaging Findings in 14 Mainland Chinese Patients with Oculopharyngodistal Myopathy

Oculopharyngodistal myopathy (OPDM) is an extremely rare, adult-onset hereditary muscular disease characterized by progressive external ocular, pharyngeal, and distal muscle weakness and myopathological rimmed vacuole changes. The causative gene is currently unknown; therefore, diagnosis of OPDM is...

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Podrobná bibliografie
Vydáno v:PLoS One
Hlavní autoři: Zhao, Juan, Liu, Jing, Xiao, Jiangxi, Du, Jing, Que, Chengli, Shi, Xin, Liang, Wei, Sun, Weiping, Zhang, Wei, Lv, He, Yuan, Yun, Wang, Zhaoxia
Médium: Artigo
Jazyk:Inglês
Vydáno: Public Library of Science 2015
Témata:
Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4454561/
https://ncbi.nlm.nih.gov/pubmed/26039504
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0128629
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