MDS Abstracts

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

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  • MDS Virtual Congress 2021

    Yoga for Functional Neurological Disorder – Two Case Descriptions

    D. Kipnis, H. Shah, L. Quinn (New York, USA)

    Objective: To describe key components of a yoga program for two individuals with Functional Neurological Disorder (FND). Background: FND is the second most common reason…
  • MDS Virtual Congress 2021

    Neuro-Behavioral Therapy for Functional Movement Disorders: Conceptual Framework and Future Directions

    J. Mack, WC. Lafrance, JR. (Portland, USA)

    Objective: To explore modifications to an established, evidence-based psychological treatment for patients with psychogenic non-epileptic seizures (PNES) with the goal of studying a manualized psychotherapy…
  • MDS Virtual Congress 2021

    Association between adverse childhood experiences and functional seizures among FND patients in the FND Patient Registry

    B. Mildon, E. Snow, J. Occean, N. Agu, A. Salinas-Miranda (Salmon, USA)

    Objective: This analysis examined the association between adverse childhood experiences (ACE) and functional seizures among FND patients. Background: Functional seizures are seizures of undetermined organic…
  • MDS Virtual Congress 2021

    Increased prevalence of obsessive-compulsive symptoms in functional movement disorders

    L. Novakova, J. Anyz, Z. Forejtová, M. Slovak, T. Rosikova, G. Vechetova, E. Ruzicka, T. Serranova (Prague, Czech Republic)

    Objective: To establish frequency of self-reported obsessive-compulsive symptoms (OCS) in patients with functional movement disorders (FMD). Background: FMD are associated with a high prevalence of…
  • MDS Virtual Congress 2021

    Excessive directional antisaccade errors in Tourette Syndrome with Attention-deficit Hyperactivity Disorder: a case report

    DSL. Sandoval-Lopez, JOM. Ortega-Márquez, DPP. Pérez-Plascencia, DCJ. Chapa-Juárez, COA. Ortéga-Arenas, AAS. Armas-Salazar (Mexico City, Mexico)

    Objective: To describe a case of a young man diagnosed with Tourette Syndrome and Attention-Deficit Hyperactivity Disorder, where oculomotor tics were observed as the main…
  • MDS Virtual Congress 2021

    Psychogenic movement disorders precipitated by post-lockdown return to school in adolescents: case series from Kenya

    D. Sokhi, K. Oyieke, P. Samia (Nairobi, Kenya)

    Objective: To describe three cases who presented with new-onset psychogenic movement disorders (PMD) after returning to school when the national lockdown was lifted. Background: PMD…
  • MDS Virtual Congress 2021

    HSP-SPG5A/CYP7B1: unusual clinical and genetic characteristics in an Indian family

    A. Orlacchio, M. Stasi, A. Stigliano, A. Meyyazhagan, T. Kawarai (Rome, Italy)

    Objective: To carry out a clinical and genetic study of a large Indian family emigrated in Italy with autosomal dominant hereditary spastic paraplegia (ADHSP). Background:…
  • MDS Virtual Congress 2021

    Differential methylation signatures in Lewy body dementia

    P. Reho, TG. Beach, GE. Serrano, KL. Newell, HP. Easwaran, JC. Troncoso, O. Pletnikova, SW. Scholz (Bethesda, USA)

    Objective: This study aimed to compare the DNA methylome of Lewy body dementia (LBD) patients and healthy controls. Background: LBD is the second most common…
  • MDS Virtual Congress 2021

    New presenilin-1 missense variant (p.Pro88Arg) characterized by initial progressive supranuclear palsy like phenotype.

    Q. Thomas, S. Nambot, C. Thauvin-Robinet, C. Philippe, Y. Bejot, G. Dupont (Dijon, France)

    Objective: To report a new presenilin-1 (PSEN 1) missense variant (p.Pro88Arg) characterized by initial Progressive Supranuclear Palsy (PSP) like phenotype. Background: Pathogenic variants in the PSEN1gene…
  • MDS Virtual Congress 2021

    Mutation analysis of BSN gene in patients with multiple system atrophy

    M. Wakita, A. Nagai, H. Yaguchi, I. Yabe (Sapporo, Japan)

    Objective: To investigate the mutations of the BSN gene in patients with multiple system atrophy (MSA). Background: We have reported some mutations in the bassoon…
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