Abstract
Oculopharyngeal Muscular Dystrophy is a rare genetic disorder characterized clinically by ptosis and deglutition difficulties. This work aims to give a detailed description of a particular case highlighting the relevance of the electromyographic findings in addition to a comprehensive literature review on the topic. Clinical, neurophysiological and molecular study of 82 years old patient referred to Clinical Neurophysiology Unit for progressive bilateral ptosis and dysphagia. The electromyographic study aimed the existence of a facial myopathy prevalence and molecular study confirmed the existence of a pathological expansion of 12 repetitions in the poly-alanine tract PABPN1 gene. Conclusions: Oculopharyngeal Muscular Dystrophy is an underdiagnosed disease that may go unnoticed by simulating other pathological processes. A rigorous neurophysiological study is essential to conduct a suspected diagnosis and to guide further molecular diagnostics.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.