MDS Abstracts

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

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Articles tagged "Chorea (also see specific diagnoses, Huntingtons disease, etc): Clinical features"

  • 2018 International Congress

    Driving performance of Huntington’s disease gene carriers

    M. Jacobs, E. Hart, Y. Mejia Miranda, G.J. Groeneveld, J. van Gerven, R. Roos (Leiden, Netherlands)

    Objective: To investigate if differences in driving performance between Huntington's disease (HD) gene carriers and healthy individuals can be detected with a driving simulator. Furthermore,…
  • 2018 International Congress

    Education in hyperkinetic movement disorders in Cameroonian health providers

    M.H.G. Monje, M.M. Kurtis, M. Molina, C. Delgado-Suárez, P. Gómez-Iglesias, I. García-Morales, D. García-Azorín (Móstoles, Madrid, Spain)

    Objective: To evaluate the educational gaps in hyperkinetic movement disorders among a widely-varied sample of Cameroonian health providers and improve understanding through a practical training…
  • 2018 International Congress

    Malignant gliomas in patients with Huntington’s disease

    S. Chandra, G. Suarez-Cedeno, E. Stimming (Houston, TX, USA)

    Objective: Discuss the presentation of glioblastoma multiforme in patients with Huntington’s disease Background: Huntington’s disease (HD) is an inherited neurodegenerative disorder caused by a trinucleotide…
  • 2018 International Congress

    The History of Huntington Disease Description in Russia

    D. Labunskiy (Santa Rosa, CA, USA)

    Objective: The report provides detailed material on the history of the description of Huntington's disease (HD) in Russia. The first, unknown to a wide audience,…
  • 2018 International Congress

    Assessing the potential of EEG as a biomarker in Huntington’s disease using machine learning automatic classification

    O. Odish, K. Johnsen, P. van Someren, R. Roos, G. van Dijk (Leiden, Netherlands)

    Objective: To construct an automatic classifier distinguishing healthy controls from Huntington’s disease (HD) gene carriers using quantitative electroencephalography (qEEG) and to derive qEEG features that…
  • 2018 International Congress

    Generalized choreoathetoid-like movements in primary Sjögren syndrome

    N. Alvarado-Franco, L. Olguín-Ramírez, A. Garza-Alpirez, G. Femat-Roldan, D. Martinez-Ramirez (Monterrey, Mexico)

    Objective: To report a case of choreoathetoid-like movements associated to primary Sjögren syndrome. Background: Autoimmune diseases are not uncommon causes of movement disorders. Two percent…
  • 2018 International Congress

    Late onset Huntington’s disease in an Argentinian cohort

    M. Cesarini, J. Etcheverry, E. Gatto, J. Ziliani, G. Da Prat, N. Gonzalez Rojas, V. Parisi, G. Persi (Buenos Aires, Argentina)

    Objective: To describe the prevalence, clinical and molecular characteristics of a series of LOHD patients in an Argentinean cohort. Background: Late onset Huntington’s disease (LOHD)…
  • 2018 International Congress

    Sydenham’s Chorea: Realities and Challenges in Sub-Saharan Africa

    A. Nitcheu Woga, A. Balde, F. Sakadi, N. Tassiou, A. Bah, F. Cisse, E. Minko (Conakry, Guinea)

    Objective: The aim of this study was to describe the epidemiological, clinical, paraclinical and evolutive aspects of Sydenham's chorea. Background: Sydenham's chorea is a rare…
  • 2018 International Congress

    On the hunt for a link between genetically confirmed Huntington’s disease and Amyotrophic Lateral Sclerosis

    L. Williams, K. O'Connell, D. Burke, J. Cryan, D. McCabe (Dublin, Ireland)

    Objective: To characterise the clinical and pathologic findings of Huntington’s disease (HD) and coincident amyotrophic lateral sclerosis (ALS). Background: A 66 year old man presented…
  • 2018 International Congress

    Spinocerebellar Ataxia Type 2 Presenting with Chorea: Korean Cases

    D. Yoo, J.Y. Lee, B. Jeon (Seoul, Republic of Korea)

    Objective: To report cases of SCA2 presenting with chorea, which have not been reported in Korea Background: Spinocerebellar ataxias (SCAs) manifest ethnic and geographical differences…
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