MDS Abstracts

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

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Articles tagged "Myoclonus: Clinical features"

  • 2016 International Congress

    Topiramate responsive adult-onset opsoclonus myoclonus ataxia syndrome

    Y. Degirmenci, H. Kececi (Duzce, Turkey)

    Objective: Opsoclonus myoclonus ataxia (OMA) is a rare neurological syndrome characterized with with autoimmune background. However the exact pathophysiology is not clear. Most common underlying…
  • 2016 International Congress

    Oculopalatal myoclonus after stroke

    B. Klysz, I. Sarzynska-Dlugosz, A. Czlonkowska, I. Kurkowska-Jastrzebska (Warsaw, Poland)

    Objective: Analysis of clinical course of oculopalatal myoclonus (OPM) and MRI images of the brain. Background: OPM are rare movement disorders connected with the injury…
  • 2016 International Congress

    Ortostatic myoclonus: A report of four cases

    Z.F. Aldaajani, F.C.F. Chang, N. Mahant, S.D. Kim, V.S.C. Fung (Sydney, Australia)

    Objective: To highlight the presentation of orthostatic myoclonus and to increase awareness of this syndrome amongst neurologists and physicians. Background: Orthostatic unsteadiness (unsteadiness on standing)…
  • 2016 International Congress

    Symptomatic palatal and respiratory tremor with ataxia following fourth ventricle epidermoid cyst removal

    B.R. Barton, B. Barton (Chicago, IL, USA)

    Objective: Present rare cause of symptomatic palatal tremor and ataxia after fourth ventricle cyst removal with unusual respiratory muscle involvement. Background: Symptomatic palatal tremor (SPT)…
  • 2016 International Congress

    The interrater variability in clinical assessment of post-hypoxic myoclonus

    J.C. van Zijl, M. Beudel, J.W.J. Elting, B.M. de Jong, J. van der Naalt, W.M. van den Bergh, A.O. Rossetti, M.A.J. Tijssen, J. Horn (Groningen, Netherlands)

    Objective: To investigate the interrater variability in clinical assessment of acute post-hypoxic myoclonus (PHM) after cardiopulmonary resuscitation. Background: PHM is a clinical symptom that can…
  • 2016 International Congress

    Persistent myoclonic dystonia due to SCL2A1 mutation

    P.H. McNamara, D. Olszewska, A. McCarthy, J. McKinley, T. McVeigh, T. Lynch (Dublin, Ireland)

    Objective: We present a young woman with myoclonic dystonia due to a novel mutation in SCL2A1 gene. Background: Mutations in the SCL2A1 gene can cause…
  • 2016 International Congress

    Children with idiopathic tics reveal additional features of hyperkinetic movement disorders

    P.F. Sinnige, R. Brandsma, W. Eggink, M.J. Kuiper, I.J. Lunsing, M. Boon, C.C.S. Delnooz, M.E. van Egmond, O.G.F. Sinnige, J.J. de Vries, P.J. Hoekstra, D.A. Sival (Groningen, Netherlands)

    Objective: To investigate whether children with tics reveal features of additional hyperkinetic movement disorders. Background: The patho-physiology for idiopathic tic disorders is unknown, although underlying…
  • 2016 International Congress

    Cognitive and behavioral problems in children and adolescents with myoclonus dystonia

    M.A. Coenen, H. Eggink, H. van den Berg, J.M. Spikman, M.A. Tijssen (Groningen, Netherlands)

    Objective: To compare the neuropsychological and behavioral profile of A) children and adolescents with myoclonus dystonia (MD) to a healthy control group and B) MD…
  • 2016 International Congress

    Alternating hemiplegia of childhood (AHC) as a new presentation of adenylate cyclase 5 (ADCY5)-mutation-associated disease

    C. Max, A. Westenberger, N. Brueggemann, A. Domingo, K. Gruetz, H. Pawlack, A. Weissbach, A.A. Kuehn, J. Spiegler, A.E. Lang, J. Sperner, V.S.C. Fung, J. Schallner, G. Gillessen-Kaesbach, A. Muenchau, C. Klein (Lübeck, Germany)

    Objective: To expand and determine the clinical spectrum associated with mutations in the Adenylate Cyclase 5 gene (ADCY5). Background: Recently, mutations in the ADCY5 gene…
  • 2016 International Congress

    Overlapping corticobasal syndromes: The many faces of the Armstrong criteria

    A. Pilotto, W. Maetzler, M. Synofzik, E. Schaeffer, C. Schulte, M.A. Hobert, K. Srulijes, T. Gasser, D. Berg (Tübingen, Germany)

    Objective: To evaluate the prevalence and clinical presentation of corticobasal variants listed in the new Armstrong criteria, exploring their overlap with progressive supranuclear palsy (PSP),…
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