MDS Abstracts

Abstracts from the International Congress of Parkinson’s and Movement Disorders.

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Articles tagged "Myoclonus: Clinical features"

  • 2023 International Congress

    Jaw opening myoclonus in Subacute Sclerosing Panencephalitis: A new phenotypic observation which may be a diagnostic clue

    D. Garg, S. Sharma (New Delhi, India)

    Objective: We aimed to study the frequency of jaw myoclonus in subacute sclerosing panencephalitis (SSPE). Background: SSPE is a rare disorder due to mutant measles…
  • 2023 International Congress

    Atypical Manifestations of Subacute Sclerosing Panencephalitis (SSPE): A Case Series from India

    G. Harikrishna, K. Mala, SK. Kodapala (MANDYA, India)

    Objective: To report unusual manifestations Subacute Sclerosing Panencephalitis. Background: Subacute Sclerosing Panencephalitis (SSPE) is a slow viral infection caused by measles virus resulting in progressive…
  • 2023 International Congress

    COVID-19 associated opsoclonus myoclonus ataxia syndrome

    K. Petrosyan, L. Martirosyan, A. Papoyan, A. Ashughyan, S. Voskanyan (Yerevan, Armenia)

    Objective: To present a rare neurological syndrome as a potential parainfectious complication of SARS-CoV-2 infection. Background: Օpsoclonus myoclonus syndrome (OMS) is rare complication of the…
  • 2023 International Congress

    Creutzfeldt-Jakob Disease misdiagnosed as Corticobasal degeneration

    M. Elkasaby, C. Duffy, B. Appleby (Cleveland, USA)

    Objective: We described clinical, radiologic, and neuropathological findings of a patient with Creutzfeldt-Jakob Disease who presented antemortem with clinical features suggestive of corticobasal degeneration. Background:…
  • 2023 International Congress

    Myoclonus Phenomenology and its Response to Antiepileptic drugs in Patients with Sub acute Sclerosing Pan encephalitis

    S. Pandey, K. Db, R. Garg, H. Malhotra, A. Jain, S. Kumar (LUCKNOW, India)

    Objective: To assess myoclonus phenomenology and its response to antiepileptic drugs in patients with SSPE. Background: Myoclonus is one of the characteristic features of Sub…
  • 2023 International Congress

    Movement disorders in children with progressive myoclonic epilepsies

    M. Ben Hafsa, H. Benrhouma, M. Jamoussi, T. Ben Younes, Z. Miladi, A. Zioudi, H. Klaa, I. Kraoua, I. Ben Youssef-Turki (Tunis, Tunisia)

    Objective: To analyze the clinical aspects, radiological features and evolution of myoclonus and other movement disorders (MD) in children with progressive myoclonic epilepsies (PMEs). Background:…
  • 2023 International Congress

    Rapidly progressive dementia – catatonia – myoclonus in 80 years old patient: An unusual case

    DAN. Rebolledo Garcia, ART. Cadena Fernandez, ANA. Michel Chavez, JUA. Calderon Martinez, HOR. Senties Madrid, GRI. Romero Sanchez (Mexico City, Mexico)

    Objective: Objective:Sporadic Creutzfeldt-Jakob Disease (sCJD) will be challenging to differentiate from other diseases, like NMDA autoimmune encephalitis (AE). The classic rapidly progressive dementia phenotype that…
  • 2023 International Congress

    Opsoclonus Myoclonus Syndrome due to subdural hematoma: an uncommon etiology

    V. Arca, F. Cavalcante, M. Saraiva, M. Bezerra (Recife, Brazil)

    Objective: . Background: Introduction:Opsoclonus myoclonus syndrome is characterized by myoclonic jerks and ocular opsoclonus (spontaneous, arrhythmic, and conjugate ocular saccades that occur in all directions…
  • 2022 International Congress

    Secondary generalized myoclonus resulting from brainstem ischemic lesion

    S. Saaf, A. Miqdadi, S. Lhassani, M. Hakimi, J. Aasfara, A. Hazim (Casablanca, Morocco)

    Objective: To report the case of a patient who developed generalized myoclonus revealing ischemic lesions of the brainstem Background: Myoclonus is a movement disorder defined…
  • 2022 International Congress

    Progressive ataxia and palatal tremor due to a novel heterozygous GRIN2A mutation

    E. Ardila, G. Kägi, F. Brugger (St. Gallen, Switzerland)

    Objective: Describe the case of a patient with adult-onset progressive ataxia and palatal tremor (PAPT) in association with a novel heterozygous mutation of the GRIN2A…
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