这个词是什么意思？
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.
中文名称索引；定义为 MeSH 英文原文，尚未逐条译审。MESH:D039141 · MeSH 2026。
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