Oculopharyngeal muscular dystrophy as a rare cause of dysphagia

Keyphrases

• Dysphagia 100%
• Rare Cause 100%
• Oculopharyngeal muscular Dystrophy 100%
• Autosomal Recessive Inheritance 66%
• Muscular Dystrophy 16%
• Late-onset 16%
• Neurological Examination 16%
• Inheritance Pattern 16%
• Magnetic Resonance Imaging 16%
• Motility Disorders 16%
• Young Males 16%
• Aged 80 Years and over 16%
• Hypotension 16%
• DNA Analysis 16%
• Eyelid 16%
• Ptosis 16%
• Barium Swallow 16%
• Consanguinity 16%
• Cerebral Ischemic Stroke 16%
• Hypopharyngeal 16%
• Rare Disease Diagnosis 16%
• Poly(A)-binding Protein 16%

Medicine and Dentistry

• Plummer-Vinson Syndrome 100%
• Oculopharyngeal Muscular Dystrophy 100%
• Autosomal Recessive Inheritance 33%
• Autosomal Dominant Inheritance 33%
• Muscular Dystrophy 16%
• Magnetic Resonance Imaging 16%
• Physical Examination 16%
• Neurologic Examination 16%
• Hypotension 16%
• DNA Determination 16%
• Manometry 16%
• Esophagography 16%
• Ptosis 16%
• Consanguinity 16%
• Polyadenylic Acid Binding Protein 16%
• Motility Disorder 16%
• Neurological Examination 16%