MDS Abstracts

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

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  • 2019 International Congress

    Optimal treatment of geniospasm: a case report and review of the literature

    M. Hull, M. Parnes (Houston, TX, USA)

    Objective: To present a case of geniospasm in a child successfully treated with botulinum toxin injections and to review previously reported cases in the literature…
  • 2019 International Congress

    Management of life threatening dyskinesias in GNAO1 related movement disorder: two new cases and review of the literature

    M. Hull, M. Parnes (Houston, TX, USA)

    Objective: To present two cases of GNAO1 related movement disorder associated with life threatening persistent chorea successfully managed with bilateral GPi deep brain stimulation (GPi-DBS)…
  • 2019 International Congress

    Pediatric anti-N-methyl-D-aspartate receptor encephalitis associated with Coat’s-like retinal telangiectasia

    N. Kumar, D. Radhakrishnana, R. Shree, G. Madhaw, R. Samanta, S. Kumari (Rishikesh, India)

    Objective: We report a case of 5-year-old Indian boy with non-paraneoplastic anti NMDAR encephalitis associated with Coat's like retinal telangiectasia. Background: Anti-N-methyl-d-aspartate receptor (NMDAR) encephalitis…
  • 2019 International Congress

    Deep brain stimulation in children: analysis of indication, outcome and complications

    DR. Maiti (Cleveland, OH, USA)

    Objective: Deep brain stimulation for pediatric movement disorder has been contemplated much less than adult counterpart. We discuss the outcome of DBS int them  children…
  • 2019 International Congress

    MOVEMENT DISORDERS FEATURES ASSOCIATED WITH WEST SYNDROME

    FS. Ngoungoure Halima, AM. Magnerou, CV. Hotcho Nganhou, M. Ndiaye, AG. Diop (Douala, Cameroon)

    Objective: To describe the clinical, therapeutic and outcome features of movement disorders (MD) observed in children with West Syndrome (WS) at the Neurology Department of…
  • 2019 International Congress

    Opsoclonus-Myoclonus-Ataxia Syndrome – Ljubljana University Children’s Hospital clinical series

    J. Orazem Mrak, D. Osredkar, D. Neubauer (Ljubljana, Slovenia)

    Objective: Analysis of number, clinical characteristics and outcome of patients admitted to our department due to OMS in the past 25 years. Background: Opsoclonus-myoclonus-ataxia syndrome…
  • 2019 International Congress

    Spectrum of Movement disorders in pediatric immune-mediated diseases

    A. Saan, K. Linn, A. Minaye, C. Hlaing, K. Ko, H. Wintaung, N. Lin, Y. Wintaung (Yangon, Myanmar)

    Objective: To study the spectrum of movement disorders in children with immune-mediated diseases in Yangon Children Hospital, Myanmar Background: Immune-mediated diseases represent expanding conditions of…
  • 2019 International Congress

    The Clinical, Molecular and Radiographic Spectrum of Adaptor Protein Complex 4-associated Hereditary Spastic Paraplegia (AP-4-HSP): Results from the AP-4-HSP International Registry

    J. Teinert, R. Behne, M. Wimmer, A. Diplock, E. Carmody, K. Dies, D. Jensen, J. Bennett, M. Sahin, D. Ebrahimi-Fakhari (Boston, MA, USA)

    Objective: 1) To develop a registry and natural history study for AP-4-HSP; 2) to define core clinical and radiographic features; 3) to explore genotype-phenotype correlations.…
  • 2019 International Congress

    Levodopa-responsive tremor in a young child as a delayed complication of osmotic demyelination from severe hypernatremia

    L. Tochen, M. Cameron, C. Brady, M. Fleming (Washington, DC, USA)

    Objective: To describe a case of levodopa responsive tremor due to osmotic demyelination as a result of severe hypernatremia Background: Osmotic demyelination is a known…
  • 2019 International Congress

    Novel compound heterozygous mutations in the TSFM gene causes childhood-onset chorea

    CH. van Riesen, K. von Au, S. Biskup, A. Kühn, A. Kaindl, A. van Riesen (Berlin, Germany)

    Objective: To report the case of a young boy suffering from a severe hyperkinetic movement disorder caused by mutations in the recently described TSFM gene.…
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