Add to ORKGIn 1915, Taylor described a hereditary condition characterized by ""progressive vagus-glossopharyngeal paralysis with ptosis,"" stating that the disorder progressed slowly and eventually caused death by starvation. Subsequently, Victor et al. called the syndrome ""oculopharyngeal muscular dystrophy"" (OPMD). Many affected families are of French-Canadian heritage. OPMD is generally inherited as an autosomal-dominant trait, but rare autosomal-recessive cases have been reported
Oculopharyngeal muscular dystrophy (OPMD) is typically inherited in an autosomal dominant fashion an...
Oculopharyngeal muscular dystrophy is a neuromuscular disease usually presenting in the 5th or 6th d...
Oculopharyngeal muscular dystrophy is a neuromuscular disease usually presenting in the 5th or 6th d...
In 1915, Taylor described a hereditary condition characterized by ""progressive vagus-glossopharynge...
Autosomal dominant oculopharyngeal muscular dystrophy (OPMD) is an adult-onset disease which is part...
Abstract Oculopharyngeal muscular dystrophy (OPMD) is a rare cause for late-onset dysphagia. OPMD no...
Oculopharyngeal muscular dystrophy (OPMD) is an adult - onset disease that is generally inherited as...
We report the complete autopsy findings of a 60-year-old, 12th generation member of the French-Canad...
PubMed ID: 21242490Background: Oculopharyngodistal myopathy (OPDM) has been reported as a rare, adul...
Oculopharyngeal muscular dystrophy (OPMD) is an autosomal dominant disorder of late onset that commo...
Background: Oculopharyngodistal myopathy (OPDM) has been reported as a rare, adult-onset hereditary ...
Oculopharyngeal muscular dystrophy (OPMD) is an autosomal dominant muscle disorder. Occasional cases...
Oculopharyngeal muscular dystrophy (OPMD) is a late onset myopathy usually presenting in the 5th or ...
Oculopharyngeal muscular dystrophy (OPMD) is an autosomal dominant disorder of late onset that commo...
Oculopharyngeal muscular dystrophy (OPMD) is an autosomal dominant disorder of late onset that commo...
Oculopharyngeal muscular dystrophy (OPMD) is typically inherited in an autosomal dominant fashion an...
Oculopharyngeal muscular dystrophy is a neuromuscular disease usually presenting in the 5th or 6th d...
Oculopharyngeal muscular dystrophy is a neuromuscular disease usually presenting in the 5th or 6th d...
In 1915, Taylor described a hereditary condition characterized by ""progressive vagus-glossopharynge...
Autosomal dominant oculopharyngeal muscular dystrophy (OPMD) is an adult-onset disease which is part...
Abstract Oculopharyngeal muscular dystrophy (OPMD) is a rare cause for late-onset dysphagia. OPMD no...
Oculopharyngeal muscular dystrophy (OPMD) is an adult - onset disease that is generally inherited as...
We report the complete autopsy findings of a 60-year-old, 12th generation member of the French-Canad...
PubMed ID: 21242490Background: Oculopharyngodistal myopathy (OPDM) has been reported as a rare, adul...
Oculopharyngeal muscular dystrophy (OPMD) is an autosomal dominant disorder of late onset that commo...
Background: Oculopharyngodistal myopathy (OPDM) has been reported as a rare, adult-onset hereditary ...
Oculopharyngeal muscular dystrophy (OPMD) is an autosomal dominant muscle disorder. Occasional cases...
Oculopharyngeal muscular dystrophy (OPMD) is a late onset myopathy usually presenting in the 5th or ...
Oculopharyngeal muscular dystrophy (OPMD) is an autosomal dominant disorder of late onset that commo...
Oculopharyngeal muscular dystrophy (OPMD) is an autosomal dominant disorder of late onset that commo...
Oculopharyngeal muscular dystrophy (OPMD) is typically inherited in an autosomal dominant fashion an...
Oculopharyngeal muscular dystrophy is a neuromuscular disease usually presenting in the 5th or 6th d...
Oculopharyngeal muscular dystrophy is a neuromuscular disease usually presenting in the 5th or 6th d...