Recurrent Pneumonia in a Patient With Oculopharyngeal Muscular Dystrophy (OPMD) due to GCN Expansion in the PABPN1 Gene: A Diagnostic Challenge
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Oculopharyngeal muscular dystrophy (OPMD) is a rare neuromuscular disorder that may present with respiratory complications, yet it is seldom considered in this context. We report a 68-year-old institutionalized man, independent in daily activities, who present... ...