MDS Abstracts

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

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  • 2026 International Congress

    Risk factors associated with Parkinson’s disease in the DRC (Case of the Initiative Plus Hospital Center, Kinshasa)

    P. Kiatoko, R. Fure (KINSHASA, The Democratic Republic of the Congo)

    Objective: identify factors that could be associated with Parkinson's disease in Congo Background: In  DRCongo, few studies have been published on Parkinson's disease to date.At…
  • 2026 International Congress

    Digital Health, Telemedicine, and Artificial Intelligence in Parkinson’s Disease Management During COVID-19: A Narrative Review

    H. Harifi (Kenitra, Morocco)

    Objective: The objective of this narrative review was to evaluate the effectiveness of telemedicine and AI-based technologies used for the remote monitoring and management of…
  • 2026 International Congress

    Intestinal Dysbiosis in Parkinson’s Disease: Mechanisms, Clinical Implications, and Therapeutic Perspectives (2015–2025)

    H. Harifi (Kenitra, Morocco)

    Objective: This narrative review aims to consolidate research published from 2015 to 2025 regarding abnormalities in gut microbiota in patients with Parkinson’s disease, emphasizing potential…
  • 2026 International Congress

    Juvenile-Onset Parkinsonism With Bilateral Striatal Necrosis Associated With a Pathogenic MT-ND3 Mitochondrial Variant

    T. Rodríguez (Antofagasta, Chile)

    Objective: To report a case of juvenile-onset parkinsonism associated with bilateral striatal necrosis and a pathogenic MT-ND3 mitochondrial DNA variant, emphasizing an atypical mitochondrial phenotype…
  • 2026 International Congress

    Homozygous PRRT2 Frameshift Mutation Presenting with Infantile Onset Seizures and Childhood Episodic Ataxia

    P. Bhatele, P. Kukkle (Manipal, India)

    Objective: To report a rare presentation of a homozygous PRRT2 frameshift mutation manifesting as infantile-onset seizures followed by childhood episodic gait imbalance. Background: PRRT2 mutations…
  • 2026 International Congress

    Rare Variant Analysis in Parkinson’s Disease Patients Stratified by Polygenic Risk

    S. Kanagasingam, A. Balan, Z. Gan-Or, K. Senkevich (Montréal, Canada)

    Objective: To identify rare variants that may contribute to Parkinson’s disease (PD) risk in individuals whose polygenic background does not adequately explain their disease status.…
  • 2026 International Congress

    VPS13A Disease: 15 Years of Illness Awaiting a Diagnosis

    K. Manysheva, D. Makhmudova (Makhachkala, Russian Federation)

    Objective: Objective. Diagnosing a disease with movement disorders is not always easy. It is even more difficult when there is a family history of hereditary…
  • 2026 International Congress

    Paroxismal Torticollis Revealing Cervical disc Calcifications in a Child About a Case

    C. Boukadir (Benaknoun; Algiers, Algeria)

    Objective: Cervical dystonia in children is rare compared to adults (1), and is often of sequelae or genetic origin (1). The objective of our work…
  • 2026 International Congress

    Disabling Holmes Tremor Following Pontine Hemorrhage Accompanied by a Unique Constellation of Movement Disorders

    P. Cataniag, J. Cruz, J. Ong, C. Diesta, J. Oropilla, R. Teleg, K. Amamanglon, M. Mendoza (Makati City, Philippines)

    Objective: To report a case of an adult Filipino male who developed delayed complex post-stroke movement disorders following a pontine hemorrhage. Background: Holmes tremor (HT)…
  • 2026 International Congress

    Underestimation of Nighttime Sleep Symptoms in Isolated RBD is Associated with Increased Risk of Phenoconversion to Synucleinopathy: A North American Prodromal Synucleinopathy Consortium Study

    J. Ha, D. Bliwise, H. Dela Cruz, C. Xiong, T. Ferman, K. Kantarci, V. Lowe, S. Criswell, E. ST. Louis, D. Huddleston, A. Avidan, Y. Ju, M. Lim, M. Miglis, R. Postuma, A. Videnovic, B. Boeve, M. Howell, L. Trotti (Atlanta, USA)

    Objective: To determine whether mismatch between participant (PT) self-perceived and bed partner (BP)–reported sleep symptoms is associated with risk of phenoconversion to synucleinopathy. Background: Patients…
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