Teaching video neuroimages: orofacial dyskinesia and oral ulceration due to involuntary biting in neuroacanthocytosis.
نویسندگان
چکیده
A 30-year-old man with a history of generalized epilepsy presented with progressively worsening involuntary movements for 2 years. He had no family history of movement disorders. He had orofacial choreiform movements with sucking, grimacing, and neck flexion, which were exacerbated with eating. He also had oral ulcers due to involuntary biting. Blood smear showed 20% acanthocytes. Nerve conduction demonstrated sensory axonal neuropathy. MRI was negative for white matter changes and caudate atrophy. Orofacial dyskinesia (video on the Neurology® Web site at www.neurology.org), oral mutilation, and feeding dystonia are typical of chorea-acanthocytosis. Generalized seizures and axonal sensory neuropathy are associated. AUTHOR CONTRIBUTIONS All authors were involved in the diagnosis and management of the patient. Dr. Gooneratne and Dr. Weeratunga were involved in preparing the video and manuscript.
منابع مشابه
Eating dystonia in a case of neuroacanthocytosis
Neuroacanthocytosis is an autosomal recessive neurodegenerative disease, characterized by chorea, dementia, seizure, acanthocytes on peripheral blood smear and caudate atrophy on brain magnetic resonance imaging (MRI).1,2 These patients have severe orofacial dyskinesia and especially eating dystonia that causes severe eating problems and tongue and cheek biting. Eating or feeding dystonia, in c...
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ورودعنوان ژورنال:
- Neurology
دوره 82 8 شماره
صفحات -
تاریخ انتشار 2014