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Can CANVAS due to RFC1 biallelic expansions present with pure ataxia?
Hadjivassiliou, Marios; Currò, Riccardo; Beauchamp, Nick; Dominik, Natalia; Grunewald, Richard A; Shanmugarajah, Priya; Zis, Panayiotis; Hoggard, Nigel; Cortese, Andrea.
Afiliação
  • Hadjivassiliou M; Academic Department of Neurosciences, Royal Hallamshire Hospital, Sheffield Teaching Hospitals NHS Trust and University of Sheffield, Sheffield, UK m.hadjivassiliou@sheffield.ac.uk.
  • Currò R; Department of Neuromuscular Disease, UCL Queen Square Institute of Neurology, London, UK.
  • Beauchamp N; Department of Brain and Bahavioural Sciences, University of Pavia, Pavia, Italy.
  • Dominik N; Sheffield Diagnostic Genetics Service, Sheffield Children's Hospital NHS Foundation Trust, Sheffield, UK.
  • Grunewald RA; Department of Neuromuscular Disease, UCL Queen Square Institute of Neurology, London, UK.
  • Shanmugarajah P; Academic Department of Neurosciences, Royal Hallamshire Hospital, Sheffield Teaching Hospitals NHS Trust and University of Sheffield, Sheffield, UK.
  • Zis P; Academic Department of Neurosciences, Royal Hallamshire Hospital, Sheffield Teaching Hospitals NHS Trust and University of Sheffield, Sheffield, UK.
  • Hoggard N; Academic Department of Neurology, University of Cyprus, Nicosia, Cyprus.
  • Cortese A; Department of Infection, Immunity and Cardiovascular Disease, The University of Sheffield, Sheffield, UK.
J Neurol Neurosurg Psychiatry ; 95(2): 171-174, 2024 Jan 11.
Article em En | MEDLINE | ID: mdl-37414537
ABSTRACT

BACKGROUND:

Biallelic expansion of AAGGG in the replication factor complex subunit 1 (RFC1) was identified as a major cause of cerebellar ataxia, neuropathy (sensory ganglionopathy, or SG) and vestibular areflexia syndrome (CANVAS). We wanted to clarify if RFC1 expansions can present with pure ataxia and if such expansions could be responsible for some cases where an alternative diagnosis had been made.

METHODS:

We identified patients with a combination of ataxia and SG and no other cause found, patients where an alternative diagnosis had been made, and patients with pure ataxia. Testing for RFC1 expansions was done using established methodology.

RESULTS:

Among 54 patients with otherwise idiopathic sporadic ataxia without SG, none was found to have RFC1 expansions. Among 38 patients with cerebellar ataxia and SG in which all other causes were excluded, 71% had RFC1 expansions. Among 27 patients with cerebellar ataxia and SG diagnosed with coeliac disease or gluten sensitivity, 15% had RFC1 expansions.

CONCLUSIONS:

Isolated cerebellar ataxia without SG makes the diagnosis of CANVAS due to RFC1 expansions highly improbable, but CANVAS is frequently the cause of the combination of idiopathic cerebellar ataxia with SG. It is important to screen patients diagnosed with other causes of acquired ataxia and SG as a small percentage were found to have RFC1 expansions.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ataxia Cerebelar / Vestibulopatia Bilateral Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: J Neurol Neurosurg Psychiatry Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ataxia Cerebelar / Vestibulopatia Bilateral Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: J Neurol Neurosurg Psychiatry Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Reino Unido