PROPRIOSPINAL MYOCLONUS ASSOCIATED TO SARS-COV-2 RESPIRATORY INFECTION
Objective: To describe a case of propriospinal myoclonus (PM) in the setting of respiratory infection by SARS-CoV-2. Background: PM is an uncommon movement disorder characterized…Myoclonus, Tremor, and Ataxia After COVID-19 Infection
Objective: We report a case of myoclonus, tremor, and ataxia after COVID-19 infection with improvement in myoclonus after treatment with levetiracetam. Background: Neurologic manifestations of…SARS-CoV-2 Encephalopathy Presenting as Opsoclonus Myoclonus Syndrome Successfully Treated with IV Immunoglobulins
Objective: To present a case of a SARS-CoV-2 patient presenting with opsoclonus myoclonus syndrome who was successfully treated with IVIGs. Background: The COVID-19 pandemic has…Covid-19 associated Opsoclonus-Myoclonus Syndrome with encephalopathy
Objective: To investigate whether the encephalopathy associated with the opsioclonus myoclonus syndrome in COVID-19 is likely to be parainfections. Background: Adult onset opsoclonus myoclonus syndrome…Lingual myoclonus associated with brain metastasis located near the primary tongue motor cortex: case report.
Objective: To report a case of a patient with lung cancer who developed lingual myoclonus, revealing brain metastases. Background: Lingual myoclonus has been described associated…Spectrum of Movement Disorders among Children with Subacute Sclerosing Panencephalitis (SSPE): A Cross-sectional Study
Objective: We aimed to assess spectrum of movement disorders associated with pediatric SSPE. Background: Subacute sclerosing panencephalitis (SSPE) is a rare neurodegenerative disorder due to…The distinct EEG signature of celiac disease-related cortical myoclonus
Objective: To describe a novel motor cortex (M1) electroencephalogram (EEG) abnormality distinct to celiac disease (CD)-related cortical myoclonus and to explore its relationship with cerebellar-M1…An unusual phenotype of spinocerebellar ataxia type 12
Objective: To describe a case of spinocerebellar ataxia type 12 (SCA-12) with an unusual phenotype. Background: SCA-12 is a rare autosomal dominant cerebellar ataxia which…Amantadine-induced negative myoclonus in a patient with Parkinson’s disease: A case report
Objective: To report a case of amantadine-induced negative myoclonus in a patient with Parkinson’s disease. Background: Parkinson’s disease is a progressive neurodegenerative disease that involves…A retrospective analysis of clinical and electrophysiological characteristics of patients with myoclonus
Objective: We aimed to evaluate the clinical characteristics of patients with myoclonus and to identify the possible etiologies in different types of myoclonus based on…
Abstracts from the International Congress of Parkinson’s and Movement Disorders.