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Muscular Dystrophy, Oculopharyngeal
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.
Drugs by status
Phase 3 trials (1)
Phase 1 trials (1)
Organizations
Organization Involved with Phase 3 Indications (8)
Organization Involved with Phase 2 Indications (2)