Neuropathy in <scp>GAA</scp>‐<scp>FGF14</scp> Late‐Onset Cerebellar Ataxia (<scp>SCA27B</scp>): Prevalence and Characteristics

The prevalence of neuropathy in SCA27B patients was similar to that reported in the elderly general population. Neuropathies were predominantly non-specific length-dependent axonal neuropathies, primarily driven by aging and known risk factors rather than the underlying genetic abnormality.

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Publication Details

Journal
European Journal of Neurology
Published
2025-06-27
DOI
https://doi.org/10.1111/ene.70247
Citations
5
Primary Topic
Genetic Neurodegenerative Diseases
Type
article
Field-Weighted Citation Impact
4.55

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article

Neuropathy in GAA‐FGF14 Late‐Onset Cerebellar Ataxia (SCA27B): Prevalence and Characteristics

Nicolas Carrière, Julian Theuriet, Sacha Weber, Virginie Guillet‐Pichon et al.
5 citations
European Journal of Neurology
Genetic Neurodegenerative Diseases
4.55
article

Neuropathy in GAA‐FGF14 Late‐Onset Cerebellar Ataxia (SCA27B): Prevalence and Characteristics

Nicolas Carrière, Julian Theuriet, Sacha Weber, Virginie Guillet‐Pichon, Jean‐Baptiste Chanson, Chloé Angelini, Gwenaël Le Guyader, Pierre Lardeux, Armand Hocquel, Bertrand Degos, Alexandra Dürr, Frédérique Fluchère, Mathilde Renaud, Emmanuel Flamand Roze, Camille Comet, Audrey Riou, Stéphane Thobois, Clément Desjardins, Cécilia Marelli, Lucie Guyant‐Marechal, Chloé Laurencin, Vincent Schneider, Antoine Pégat, Adrian Degardin, Guillemette Clément, Céline Bonnet, Cyril Goizet, Caroline Froment Tilikete, E. Besse-Pinot, Brice Laurens, Fabienne Ory‐Magne, Quentin Thomas, Gwendoline Dupont, Aurélie Méneret, Jean‐Philippe Azulay, Sandra Mercier, Anna Heinzmann, Blandine Acket, Mathieu Anheim, Thomas Wirth, Claire Ewenczyk, Manon Degoutin, Christophe Verny, Françoise Bouhour, Giulia Coarelli, Lukas Paulet, Maxime Merindol, Hocine Belbachir
article en
5 citations

Abstract

The prevalence of neuropathy in SCA27B patients was similar to that reported in the elderly general population. Neuropathies were predominantly non-specific length-dependent axonal neuropathies, primarily driven by aging and known risk factors rather than the underlying genetic abnormality.

European Journal of NeurologyVol. 32(7)
Université Claude Bernard Lyon 1 (FR), Centre National de la Recherche Scientifique (FR), Inserm (FR), École Pratique des Hautes Études (FR), Université de Montpellier (FR), Centre Hospitalier Universitaire de Bordeaux (FR), Centre Hospitalier Universitaire de Lille (FR), Centre Hospitalier Universitaire de Nantes (FR), Centre Hospitalier Universitaire de Toulouse (FR), Sorbonne Université (FR), Institut de génétique et de biologie moléculaire et cellulaire (FR), Assistance Publique Hôpitaux de Marseille (FR), Centre de Recherche en Neurosciences de Lyon (FR), Assistance Publique – Hôpitaux de Paris (FR), Centre Hospitalier Régional et Universitaire de Nancy (FR), Hospices Civils de Lyon (FR), Hôpital Roger Salengro (FR), Hôpital Pierre Wertheimer (FR), Centre Hospitalier Universitaire de Poitiers (FR), Hôpital Pellegrin (FR), Centre Hospitalier Universitaire d'Angers (FR), Centre de Physiopathologie de Toulouse-Purpan (FR), Centre Hospitalier Universitaire de Caen Normandie (FR), CHU Dijon Bourgogne (FR), CIC Rennes (FR), Centre Hospitalier Universitaire de Limoges (FR), Fondation Ophtalmologique Adolphe de Rothschild (FR), Institut NeuroMyoGène (FR), Centre Hospitalier Universitaire de Clermont-Ferrand (FR), Hôpital Avicenne (FR), Hôpitaux Universitaires de Strasbourg (FR), Services déconcentrés d'appui à la recherche Occitanie-Montpellier (FR), Institut du Cerveau (FR), Centre Hospitalier Universitaire de Rouen (FR), Centre Hospitalier Universitaire de Rennes (FR), Hôpital de la Timone (FR), Nutrition-Génétique et Exposition aux Risques Environnementaux (FR), Université de Rouen Normandie (FR), Université de Strasbourg (FR), Université de Lorraine (FR), Université de Caen Normandie (FR)
China Scholarship Council, Centre Hospitalier Régional Universitaire de Montpellier, Hospices Civils de Lyon
Good health and well-being
Openalex Percentile: Top 5%
Genetic Neurodegenerative Diseases
4.55
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