MDS Abstracts

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

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Articles tagged "Dystonia: Genetics"

  • MDS Virtual Congress 2021

    GNAO1 related movement disorders: 2 longitudinally-followed cases

    CC. Wang, S. Lee (Lebanon, USA)

    Objective: To describe the clinical course, phenomenology, and treatment response in two patients with GNAO1 related movement disorders. Background: Since the initial report of 4…
  • MDS Virtual Congress 2021

    A new mutation in the C-terminal domain of the YY1 gene associated with Gabriele-de Vries syndrome.

    J. Gamez, M. Garcia-Hoyos, O. de Fabregues (Sant Just Desvern, Spain)

    Objective: To report a new mutation in the YY1 gene in a patient with Gabriele-de Vries syndrome, in which dystonia and choreoathetosis were the most…
  • MDS Virtual Congress 2021

    Deep Brain Stimulation for Dystonia: A Single-center Experience

    S. Carr, T. Herrington, M. Supnet, X. Al Qahtani, P. Acuna, K. Kanoff, C. Wahle, N. Sharma, E. Penney (Charlestown, USA)

    Objective: To report on deep brain stimulation (DBS) outcomes in dystonia and related movement disorders at Mass General Brigham (MGB) hospitals. Background: Dystonia is a…
  • MDS Virtual Congress 2021

    Combined dystonia in a patient carrying a novel ATL1 gene variant.

    M. Gea, K. Beyer, F. Nuñez, L. Ispierto, R. álvarez, G. Lucente, D. Vilas (Badalona, Spain)

    Objective: To describe a patient with a childhood-onset combined dystonia who was found to be a carrier of a novel mutation in the ATL1 gene.…
  • MDS Virtual Congress 2021

    Successful bilateral pallidal stimulation in a young adult with DYT-27: A case report

    M. Nguyen, S. Khandhar, M. Anderson, P. Pezeshkian, M. Sedrak, R. Ceponiene (Elk Grove, USA)

    Objective: We present a 21 year old woman with DYT-27 dystonia who received bilateral pallidal deep brain stimulation. Background: Dystonia is a neurological disorder characterized…
  • MDS Virtual Congress 2021

    Molecular changes of a de novo missense variant in VPS16 in dystonia

    H. Pott, K. Zeuner, C. örün, S. Paschen, S. Diaw, K. Plötze-Martin, M. Borsche, G. Kuhlenbäumer, C. Klein, N. Brüggemann, M. Klinger, K. Lohmann (Lübeck, Germany)

    Objective: To present an early-onset dystonia patient with a de novo VPS16 missense variant, along with molecular characterization. Background: Mutations of the adaptor protein vacuolar…
  • MDS Virtual Congress 2021

    Pallidal Stimulation in children with monogenic dystonia

    A. Salazar Villacorta, M. Tardáguila, A. Bescós, K. Rosas, I. Delgado, L. Ispierto, R. álvarez, J. Muñoz, M. Poca, B. Pérez (Barcelona, Spain)

    Objective: To evaluate the efficacy and safety of Globus Pallidus Internus deep brain stimulation (GPi-DBS) in children with different forms of monogenic dystonia operated by…
  • MDS Virtual Congress 2021

    GPi-DBS for KMT2B-associated dystonia: systematic review and meta-analysis

    A. Saini (New Deelhi, India)

    Objective: To determine the efficacy of pallidal stimulation and GPi-DBS in KMT2B-associated dystonia. Background: Early evidence suggests good response to pallidal stimulation in KMT2B dystonia,…
  • MDS Virtual Congress 2021

    Deep Brain Stimulation in Confirmed Genetic Dystonias: A Comprehensive Review

    H. Sarva, F. Rodriguez-Porcel, S. Barkan, E. Gatto, P. Garcia Ruiz (New York, USA)

    Objective: Review DBS benefit in genetically confirmed dystonias. Background: Deep brain stimulation (DBS) is an established option for genetic dystonias such as DYT-1. While literature…
  • MDS Virtual Congress 2021

    Whole genome sequencing aids in diagnosing GCH1 dopa responsive dystonia in two Peruvian patients and influences medical management

    L. Urbina-Ramirez, J. La Serna-Infantes, E. Sarapura-Castro, A. Rivera-Valdivia, E. Thorpe, D. Perry, K. Milla-Neyra, C. Galarreta, M. Dueñas-Roque, M. Cornejo-Olivas (Lima, Peru)

    Objective: To describe the clinical features and treatment response of two Peruvian patients with GHC1 dopa responsive dystonia diagnosed by whole genome sequencing. Background: Pathogenic variants in…
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