MDS Abstracts

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

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Articles tagged "Dystonia: Treatment"

  • MDS Virtual Congress 2020

    Unlocking dystonia from Parkinson’s disease (PD) with directional deep brain stimulation (DBS)

    R. Vaden, A. Nakhmani, C. Hurt, C. Gonzalez, B. Guthrie, H. Walker (Birmingham, AL, USA)

    Objective: To investigate dystonia associated with PD in patients undergoing unilateral subthalamic nucleus (STN) DBS implantation. Background: Dystonia is a twisting, involuntary movement that often…
  • MDS Virtual Congress 2020

    Stimulation induced dystypia after pallidal deep brain stimulation

    J. Wong, M. Armstrong, L. Almeida, M. Okun, I. Malaty (Gainesville, FL, USA)

    Objective: _ Background: Typing on a keyboard requires complex collaboration between visuospatial procedural memory, language and motor function [1,2]. The impaired ability to type, independent…
  • MDS Virtual Congress 2020

    Pridopidine for the Treatment of Early Huntington’s Disease

    M. Geva, R. Reilmann, C. Olanow, M. Leinonen, Y. Cohen, P. Meyer, A. McGarry, O. Sabri, M. Hayden, K. Kieburtz (Herzliya, Israel)

    Objective: Assess the efficacy of pridopidine 45 mg bid for maintenance of total functional capacity (TFC) and motor function in early HD patients. Background: Pridopidine…
  • MDS Virtual Congress 2020

    KMT2B-related dystonia (DYT28) and Klippel-Feil Syndrome: A new association?

    D. Portela, M. Correa, M. Gomes, G. Noleto, C. Costa, J. Lopes, L. de Oliveira (Teresina, Brazil)

    Objective: To report the association of lysine-specific histone-methyltransferase 2B gene (KMT2B)-related dystonia (DYT28) and Klippel-Feil Syndrome (KFS). Background: Dystonia is a hyperkinetic movement disorder characterized…
  • MDS Virtual Congress 2020

    Self-Perception of Dysphagia Before and After Botulinum Toxin Injection for Cervical Dystonia

    A. Silbergleit, K. Hamilton, L. Schultz, J. Turnbull, E. Boettcher, R. Konnai, N. Patel, C. Sidiropoulos (West Bloomfield, MI, USA)

    Objective: To determine if individuals with cervical dystonia perceive changes in swallowing skills following botulinum toxin (BoTN) injection. Background: Cervical dystonia (CD) is known to…
  • MDS Virtual Congress 2020

    Sexual dysfunction associated with deep brain stimulation of the Globus Pallidus pars interna

    T. Fay-Karmon, G. Bronner, S. Hassin-Baer, S. Israeli-Korn (Ramat-Gan, Israel)

    Objective: To explore sexual dysfunction (SD) in a dystonia patient with deep brain stimulation of the Globus Pallidus pars interna (GPi DBS). Background: There is…
  • MDS Virtual Congress 2020

    Tardive Dystonia Successfully treated with DBS

    M. Ferreira Cordellini, D. Benzecry Almeida (Curitiba, Brazil)

    Objective: To demonstrate a successful treatment of neuroleptic-induced generalized dystonia with DBS Background: Male patient, 30 years old. At thirteen years of age, was diagnosed…
  • MDS Virtual Congress 2020

    Non-Staged Bilateral GPi DBS Lead Revision Using iMRI: A Case Report

    B. Hwang, D. Mampre, K. Mills, A. Butala, W. Anderson (Baltimore, MD, USA)

    Objective: To demonstrate the feasibility of non-staged intraoperative MRI (iMRI) deep brain stimulation (DBS) lead revision under general anesthesia (GA). Background: DBS lead revision surgery…
  • MDS Virtual Congress 2020

    Refractory cervical dystonia: is the infiltration of the obliquus capitis inferior muscle a game changer?

    A. Beltrán, F. Rodríguez, J.L Chico García, P. Parra, I. Pareés, J.C Martínez Castrillo, A. Alonso Cánovas, G. Sánchez (Madrid, Spain)

    Objective: To communicate the results of infiltration of obliquus capitis inferior (OCI) muscle in complex cervical dystonia (CD). Background: Treatment of CD with botulinum toxin…
  • MDS Virtual Congress 2020

    Bilateral GPi DBS for the treatment of severe generalized genetic dystonia caused by KMT2B mutation (DYT-28)

    J. Lopez-Castellanos, M. Lotia (Little Rock, AR, USA)

    Objective: . Background: KMT2B-related dystonia (DYT-28) is a complex childhood-onset movement disorder, characterized by a limb onset dystonia progressing to generalized dystonia with cranio-cervical involvement…
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