https://pubmed.ncbi.nlm.nih.gov/11222452/
Oculopharyngeal muscular dystrophy: phenotypic and genotypic studies in a UK population
Oculopharyngeal muscular dystrophy (OPMD) is an autosomal dominant disorder of late onset that commonly presents with ptosis and dysphagia. The genetic basis...
muscular dystrophy
https://eprints.ncl.ac.uk/253838
Muscle MRI in a large cohort of patients with oculopharyngeal muscular dystrophy - ePrints -...
https://www.semanticscholar.org/topic/Muscular-Dystrophy%2C-Oculopharyngeal/345834
Muscular Dystrophy, Oculopharyngeal | Semantic Scholar
An autosomal dominant hereditary disease that presents in late in life and is characterized by DYSPHAGIA and progressive ptosis of the eyelids. Mutations in...
muscular dystrophysemanticscholar