Ear Dyskinesia in the Absence of Neuroleptics: A Case Report
Mohammed Azzahrani, Abeer Algasim

TL;DR
A rare case of ear dyskinesia without neuroleptic use is reported, highlighting its unusual symptoms and treatment challenges.
Contribution
This is a rare case report of ear dyskinesia occurring without neuroleptic exposure, expanding clinical understanding of the condition.
Findings
The patient exhibited non-rhythmic, unilateral ear and head muscle contractions over a year.
Botulinum toxin treatment was ineffective, and the patient was lost to follow-up.
No underlying pathology was found, emphasizing the need for further research on this condition.
Abstract
Ear dyskinesia, also known as "moving ear syndrome," is a rare movement disorder characterized by involuntary, rhythmic, or semi-rhythmic contractions of the external ear muscles. The condition is not well-documented in the medical literature, with only a few case reports available. We present the case of a 37-year-old teacher from Saudi Arabia who developed a history of sudden, progressive involuntary movement of the posterior head region, provoking movement of the external ears, over the course of one year. The movements were non-rhythmical, more prominent on the right side, and associated with occasional involvement of the face and anterior neck muscles. The patient had no history of neuroleptic use or other relevant medical conditions. Examination confirmed the presence of palpable muscle contractions originating mainly from the posterior region, with the movements not synchronized…
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Taxonomy
TopicsBotulinum Toxin and Related Neurological Disorders · Trigeminal Neuralgia and Treatments · Parkinson's Disease Mechanisms and Treatments
