2026 International Congress » Ataxia

Meeting: 2026 International Congress

A Case of Progressive Cerebellar Syndrome with Ataxia as a First Sign

J. Mateo, A. Tamayo (Callao, Peru)

A Case of Rapidly Evolving Ataxic Syndrom in a Young Adult

J. Mateo, A. Beteta (Callao, Peru)

A case series of Spinocerebellar ataxia subtype 15 from Chile

M. Niedbalski, M. Canals, F. Urbina, M. Leon, S. de Almorzara, M. Sánchez, M. Miranda (Santiago, Chile)

Ambulatory prognosis in spinocerebellar ataxia type 6: a single-center cohort study

J. Nunomura (Aomori, Japan)

Assessment of GCA repeat expansion in the GLS gene among Indian patients with Spinocerebellar Ataxia

V. Suroliya, M. Kumar, B. Uppili, AK. Srivastava, M. Faruq (Gurugram, India)

Ataxia as the Primary Symptom of Leber Hereditary Optic Neuropathy: A Case Report of a Patient and Family Observation

D. Korotkova, M. Karpova (Chelyabinsk, Russian Federation)

Blood glucose homeostasis is conserved in patients with mild to moderate Spinocerebellar Ataxia type 2

R. Aguilera-Rodríguez, D. Almaguer-Gotay, A. álvarez-Sosa, M. Anidos-Machado, Y. Silva-Ricardo, D. Cuello-Almarales, A. Estupiñán-Rodríguez, L. Almaguer-Mederos (Holguín, Cuba)

Clinical and genetic analysis of Kuwaiti and Saudi families exhibiting CLN5 adult-onset autosomal recessive spinocerebellar ataxia. A potential founder mutation

W. Kamel, H. Alrohaif, M. Almannai, D. Al Mehatab, W. Aljirdrawi, L. Bastaki (Beni-Suef, Egypt)

Clinical and Genetic Characteristics of SACS-Related Ataxia: A Case Series of 13 Patients from a Consanguineous Arab Population

H. Alqahtani, F. Alqahtani, M. Abukhalid, M. Almuhaizea, S. Bohlega, S. Alshimemeri, A. Aldakheel, S. Alqahtani (Riyhadh, Saudi Arabia)

Clinical Spectrum of Cerebellar Fits in Adults and Children: A Systematic Review

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

Clinicogenetic Characterization of Sporadic Adult-Onset Ataxias in Austria

L. Schwaighofer, W. Nachbauer, M. Amprosi, D. Boesch, M. Schranz, R. Praschberger, A. Fanciulli, J. Wanschitz, S. Boesch, E. Indelicato (Innsbruck, Austria)

Cross-Sectional and Longitudinal MRI Biomarkers of Neurodegeneration in Friedreich’s Ataxia

R. Sutil Berjón, L. Manrique, F. Martínez Dubarbie, A. Pelayo Negro, N. Benitez Calle, M. Sánchez Pelaez, D. Cota González, R. Loza Palacios, R. Martínez Díaz, C. Sánchez Quintana, I. Sánchez, A. Matilla Dueñas, D. Castanedo Vázquez, M. Drake Pérez, E. Marco, C. Biarnés Duran, E. Dela Calle, J. Infante (Santander, Spain)

Disease Burden Profile of Patients with Spinocerebellar Ataxia in China: A Real-World Registry Study (2025)

LY. Lu, LF. Zhang, Y. Huang (Beijing, China)

Effects of a Six-Week Neurorehabilitation Program on Ataxia, Balance and Gait in a Patient with CANVAS Syndrome: A Case Report

M. Salamci, A. Guclu-Gunduz, M. Akbostanci (Ankara, Turkey)

Expanding the clinical and genetic spectrum of SCA15: a rare case report

M. Shah, K. Shah (Mumbai, India)

Genetic Landscape of Hereditary Ataxia in a Highly Consanguineous Population: A Nationwide Multicenter Study

F. Alqahtani, H. Alqahtani, A. Binbakheet, Z. Alqahtani, A. Sayed, A. Alsayegh, O. Alghamdi, A. Alqahtani, T. Almejaish, A. Almatrafi, A. Alhashim, A. Alotaibi, A. Kentab, R. Alshawaf, M. Abukhalid, A. Aldokheel, S. Alshimemeri, S. Alqahtani, N. Kaya, M. Rifai (Riyadh, Saudi Arabia)

Genetic modifiers of the clinical phenotype in Spinocerebellar Ataxia type 2. 25 years of candidate genes studies and the forthcoming GWAS era

L. Almaguer-Mederos (London, United Kingdom)

Genetic spectrum of spinocerebellar ataxia type 27b (atx-fgf14-gaa): a single-center study

A. Protsenko, N. Abramycheva, E. Nuzhnyi, S. Klyushnikov, S. Illarioshkin (Moscow, Russian Federation)

Genotype-Specific Risk Factors for Falls in Spinocerebellar Ataxia: A Cross-Sectional Analysis of SCA1, SCA2, SCA3, and SCA6

S. Kakde, Y. Lin, S. Kuo (Taipei, Taiwan)

GSTM1 and GSTT1 null genotypes as candidate modifiers of clinical severity and genomic instability in Cuban patients with Spinocerebellar Ataxia type 2

D. Cuello-Almarales, R. Aguilera-Rodríguez, D. Almaguer-Gotay, L. Osorio-González, L. Almaguer-Mederos (Holguin, Cuba)

Home-Based Targeted tDCS for Cerebellar Ataxia: Results of a Randomized Double-Blind Crossover Study with Remote Functional Assessment

N. Rozenberg, N. Inbar, M. Abo-Said, P. Ponger, S. Frenkel-Toledo, M. Brozgol, JM. Hausdorff, Z. Yekutieli, S. Springer, T. Gurevich (Tel Aviv, Israel)

Investigating Mitochondrial Integrity in Spinocerebellar Ataxia Type 12 via Patient-Derived iPSC Models

J. Rungta, R. Banerjee, S. Sengupta, B. Reddy, S. Ansari, R. Khatun, J. Ganguly, D. Dutta, S. Mukherjee, P. Basu, S. Choudhury, R. Pal, S. Chattarji, H. Kumar (Kolkata, India)

Late-Onset Bulbar-Predominant Neurodegeneration Associated With a Truncating AFG3L2 Variant: Expanding the Clinical Spectrum of AFG3L2-Related Disease

R. Sharma, A. Higinbotham, C. Chambers, G. Solorzano (Charlottesville, USA)

Modeling disease progression in spinocerebellar ataxias

J. Faber, E. Georgii, T. Klockgether, T. Ashizawa, K. Sheng-Han, H. Jacobi, M. Piraud (Bonn, Germany)

Omaveloxolone in a real-world setting: implications in Friedreich Ataxia beyond the classic study population

W. Nachbauer, M. Amprosi, D. Boesch, M. Schranz, E. Indelicato, L. Schwaighofer, S. Boesch (Innsbruck, Austria)

Plasma Proteomics Reveals Altered Redox Balance And Protein Homeostasis In Spinocerebellar Ataxia Type 12

S. Ansari, I. Sadaf, A. Bhardwaj, S. Haldar, J. Rungta, S. Sengupta, R. Banerjee, J. Ganguly, D. Dutta, S. Mukherjee, P. Basu, R. Pal, S. Chattarji, T. Maiti, S. Choudhury, H. Kumar (Kolkata, India)

PPP2R2B Splice Variant Dysregulation Promotes Mitochondrial Association and Neuronal Apoptosis in iPSC-Derived Neurons from Spinocerebellar Ataxia Type 12 Patient

S. Sengupta, R. Banerjee, J. Rungta, B. Reddy, S. Ansari, R. Khatun, R. Mukhopadhyay, S. Pal, J. Ganguly, D. Dutta, S. Mukherjee, P. Basu, S. Choudhury, R. Pal, S. Chattarji, H. Kumar (Kolkata, India)

Progressive Lifelong Chorea with Spastic Paraparese and Cerebellar Ataxia Associated with Two Heterozygous Variants in the SYNE1 Gene: A Case Report

I. Sarac, H. Sarac, F. Borovecki, N. Henigsberg (Zagreb, Croatia)

Shunt‑Responsive Normal Pressure Hydrocephalus in Spinocerebellar Ataxia Type 12: A Case Illustrating Treatable Neurodegenerative Overlap

R. Kaur, B. Prajapati, R. Sharma, A. Srivastava, D. Radhakrishnan (Delhi, India)

Spinocerebellar Ataxia Type 27B: A Single-Center Experience

S. Hooshmand, L. Jackson (Rochester, USA)

Targeted Repeat-Expansion Screening Highlights Unmet Genomic Needs in Genetically Naive Ataxia: A Ukrainian Single-Centre Pilot Study

S. Bandrivska, L. Mederos, N. Dominik, C. Correa, F. Magrinelli, H. Houlden, T. Slobodin (London, United Kingdom)

The Non-Motor and Extra-Cerebellar Motor Spectrum of Adult-Onset Genetic and Sporadic Cerebellar Ataxias

E. Woo, D. Abo Alsamh, V. Bruno, V. Karnik, S. Furtado (Calgary, Canada)

Transcriptomic Profiling of Frataxin-Deficient Drosophila melanogaster to Identify Molecular Drivers and Pathway Disruptions in Friedreich’s Ataxia

V. Swarup, R. Yadav, A. Ahuja, P. Yadav, A. Srivastava, D. Garg (New Delhi, India)

Triplet repeat length determines the liquid-liquid phase separation propensity of single-dtranded DNA

HJ. Yang, JI. Choi (Incheon, Republic of Korea)

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