Your browser doesn't support javascript.
loading
Does Spinocerebellar ataxia 27B mimic cerebellar multiple system atrophy?
Wirth, Thomas; Bonnet, Céline; Delvallée, Clarisse; Pellerin, David; Bogdan, Thomas; Clément, Guillemette; Schalk, Audrey; Chanson, Jean-Baptiste; Fleury, Marie-Céline; Piton, Amélie; Calmels, Nadège; Namer, Izzie Jacques; Kremer, Stéphane; Brais, Bernard; Tranchant, Christine; Renaud, Mathilde; Anheim, Mathieu.
Afiliación
  • Wirth T; Neurology Department, Strasbourg University Hospital, Strasbourg, France. thomas.wirth@chru-strasbourg.fr.
  • Bonnet C; Strasbourg Federation of Translational Medicine, Strasbourg University, Strasbourg, France. thomas.wirth@chru-strasbourg.fr.
  • Delvallée C; Institute of Genetics and Cellular and Molecular Biology, INSERM-U964, CNRS-UMR7104, University of Strasbourg, Illkirch-Graffenstaden, France. thomas.wirth@chru-strasbourg.fr.
  • Pellerin D; Medical Genetics Laboratory, Nancy Regional University Hospital, Nancy, France.
  • Bogdan T; INSERM UMR_S 1256, Nutrition, Genetics, and Environmental Risk Exposure (NGERE), Lorraine Univesity, 54000, Nancy, France.
  • Clément G; Neurology Department, Strasbourg University Hospital, Strasbourg, France.
  • Schalk A; Strasbourg Federation of Translational Medicine, Strasbourg University, Strasbourg, France.
  • Chanson JB; Institute of Genetics and Cellular and Molecular Biology, INSERM-U964, CNRS-UMR7104, University of Strasbourg, Illkirch-Graffenstaden, France.
  • Fleury MC; Department of Neurology and Neurosurgery, Montreal Neurological Hospital and Institute, McGill University, Montreal, Canada.
  • Piton A; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, University College London, London, UK.
  • Calmels N; Neurology Department, Strasbourg University Hospital, Strasbourg, France.
  • Namer IJ; Neurology Department, Nancy Regional University Hospital, Nancy, France.
  • Kremer S; Strasbourg Federation of Translational Medicine, Strasbourg University, Strasbourg, France.
  • Brais B; Genetic Diagnosis Laboratory, Strasbourg University Hospital, Strasbourg, France.
  • Tranchant C; Neurology Department, Strasbourg University Hospital, Strasbourg, France.
  • Renaud M; Strasbourg Federation of Translational Medicine, Strasbourg University, Strasbourg, France.
  • Anheim M; Neuromuscular Center Nord/Est/Ile-de-France, Strasbourg University Hospital, Strasbourg, France.
J Neurol ; 271(4): 2078-2085, 2024 Apr.
Article en En | MEDLINE | ID: mdl-38263489
ABSTRACT

BACKGROUND:

Whether spinocerebellar ataxia 27B (SCA27B) may present as a cerebellar multiple system atrophy (MSA-C) mimic remains undetermined.

OBJECTIVES:

To assess the prevalence of FGF14 (GAA)≥250 expansions in patients with MSA-C, to compare SCA27B and MSA-C clinical presentation and natural history.

METHODS:

FGF14 expansion screening combined with longitudinal deep-phenotyping in a prospective cohort of 195 patients with sporadic late-onset cerebellar ataxia.

RESULTS:

After a mean disease duration of 6.4 years, 111 patients were not meeting criteria for MSA-C while 24 and 60 patients had a final diagnosis of possible and probable MSA-C, respectively. 16 patients carried an FGF14 (GAA)≥250 expansion in the group not meeting MSA-C criteria (14.4%), 3 patients in the possible MSA-C group (12.5%), but none among probable MSA-C cases. SCA27B patients were evolving more slowly than probable MSA-C patients.

CONCLUSIONS:

FGF14 (GAA)≥250 expansion may account for MSA look-alike cases and should be screened among slow progressors.
Asunto(s)
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Degeneraciones Espinocerebelosas / Atrofia de Múltiples Sistemas / Ataxias Espinocerebelosas Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Revista: J Neurol Año: 2024 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Degeneraciones Espinocerebelosas / Atrofia de Múltiples Sistemas / Ataxias Espinocerebelosas Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Revista: J Neurol Año: 2024 Tipo del documento: Article País de afiliación: Francia