Surgical Myectomy and Myotomy for Refractory Blepharospasm in Meige Syndrome Patients: A Case Report
- PMID: 38751963
- PMCID: PMC11095178
- DOI: 10.1177/11795476241254266
Surgical Myectomy and Myotomy for Refractory Blepharospasm in Meige Syndrome Patients: A Case Report
Abstract
Meige syndrome is a rare neurological disease characterized by segmental dystonia, specifically blepharospasm and oromandibular dystonia. These symptoms are often accompanied by complex movements of the eyelids, lower facial muscles, mandible, and neck muscles. Bilateral blepharospasm is the most common feature of this disease. In this case report, we present the successful treatment of refractory blepharospasm in a 72-year-old woman with Meige syndrome via 2 incisions resulting from myectomy and in situ surgery.
Keywords: Meige syndrome; blepharospasm; myectomy; myotomy.
© The Author(s) 2024.
Conflict of interest statement
The author(s) declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: In compliance with the ICMJE uniform disclosure form, all the authors declare the following: Payment/services info: All the authors declare that no financial support was received from any organization for the submitted work. Financial relationships: All the authors declare that they have no financial relationships at present or established within the previous 3 years with any organizations that might have an interest in the submitted work. Other relationships: All the authors declare that there are no other relationships or activities that could appear to have influenced the submitted work.
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