MDS Abstracts

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

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Articles tagged "Myoclonus: Clinical features"

  • 2018 International Congress

    Clinical and genetics characterization of patients with Myoclonus Dystonia Syndrome

    B. Perez-Dueñas, M. Vanegas, L. Marti, A. Darling, D. Ortigoza-Escobar, S. Candela, H. Baide, J. Campistol, S. Aguilera, M. Marti, A. Macaya (Barcelona, Spain)

    Objective: To characterize clinically and genetically a series of 23 patients with myoclonus dystonia syndrome (MDS) and to explore the Unified Myoclonus Rating Scale (UMRS)…
  • 2018 International Congress

    Myoclonus in the pediatric age group: A retrospective analysis of clinical and electrophysiological characteristics of patients referred to an electrophysiology laboratory

    A. Gunduz, H. Yılmaz, V. Demirbilek, C. Yalçınkaya, N. Yeni, S. Saltık, M. E. Kızıltan (Istanbul, Turkey)

    Objective: We aimed to investigate clinical and electrophysiological features myoclonus in the pediatric age group. Background: Myoclonus is a movement disorder characterized by sudden, brief…
  • 2018 International Congress

    New Nomenclature Of Genetic Myoclonus Syndromes

    S. Veen, R. Zutt, C. Klein, C. Marras, S. Berkovic, J. Caviness, H. Shibasaki, T. De Koning, M. Tijssen (Groningen, Netherlands)

    Objective: In collaboration with the International Parkinson and Movement Disorder Task Force for Nomenclature of Genetic Movement Disorders, we present a new classification of genetically…
  • 2018 International Congress

    An Unusual Case of Peripheral Myoclonus

    M. de Lima (Phoenix, AZ, USA)

    Objective: To report a case of peripheral myoclonus of the lower extremity after injury. Background: Peripheral myoclonus arises as a consequence of a peripheral nervous…
  • 2018 International Congress

    Peculiarities of Opsoclonus-Myoclonus Syndrome in India: A Systematic Review of reported cases

    J. Sahu, S. Negi (Chandigarh, India)

    Objective: The aim of the study was to study the reported cases on opsoclonus-myoclonus syndrome in India and to analyze its peculiarities in comparison with…
  • 2018 International Congress

    mGluR1 antibodies encephalitis: A rare cause of reversible ataxia and myoclonus syndrome

    F. Ory Magne, C. Goillion, J. Dupouy, M. Simonetta, C. Brefel Courbon, O. Rascol, J. (Toulouse, France)

    Objective: We wanted to report the case of a patient with severe subacute cerebellar ataxia related to mGluR1-antibodies with a clear improvement after immunomodulator treatment.…
  • 2018 International Congress

    Recognise and treat functional myoclonus: Case report

    L. Tesolin, M. Liechti, S. Aybek (Trieste, Italy)

    Objective: FND account for 15% of all new patients seen in general neurology referral. Despite the burden in terms of prevalence and disability, evidence regarding…
  • 2018 International Congress

    Symptomatic Isolated Tongue Tremor of Cortical Origin Due to Stroke

    S. Thakolwiboon, D. Ruthirago, P. Laengvejkal, J. Kim, H. Wilms (Lubbock, TX, USA)

    Objective: To present an unusual case of transient, isolated tongue tremor from an ischemic stroke. Background: Isolated tongue tremor is an uncommon neurological symptom. A…
  • 2017 International Congress

    Reappraisal of Progressive Myoclonus Ataxia

    S. vd Veen, R. Zutt, T. De Koning, M. Tijssen (Groningen, Netherlands)

    Objective: To define the clinical, electrophysiological and etiological features of progressive myoclonus ataxia (PMA). Background: PMA, formerly known as the Ramsay Hunt syndrome, is a…
  • 2017 International Congress

    Clinical and electrophysiological features of seven patients with moving toes syndrome: Is it a type of spinal segmental myoclonus?

    G. Kiziltan, H. Kurucu, C. Yalcinkaya, A. Gunduz, M. E. Kiziltan (Istanbul, Turkey)

    Objective: We aimed to present a case series of moving toes syndrome to show how clinical presentation and electrophysiological findings may change. Background: The moving…
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