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Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansion

Authors :
Tanya Stojkovic
Thierry Maisonobe
Henry Houlden
Stefano Tozza
Riccardo Currò
Wai Yan Yau
Zoe Dyer
Stephan Züchner
Nigel G. Laing
Lea Leonardis
Paola Giunti
Phillipa J. Lamont
Gilbert J Thomas-Black
Roisin Sullivan
Wilson Marques
Stephanie Efthymiou
Salvatore Rossi
Patrick F. Chinnery
Andrea Cortese
Sarah J. Beecroft
Andrew Chancellor
Diego Kaski
Menelaos Pipis
Richard Roxburgh
Pedro J. Tomaselli
Gianina Ravenscroft
Matilde Laura
Alexander M. Rossor
Alejandro Horga
Cristina Tassorelli
James M. Polke
Adolfo M. Bronstein
Yann Péréon
Giulia Mallucci
Mary M. Reilly
Silvia Colnaghi
Rita Horvath
Stuart Mossman
Zane Jaunmuktane
Nicholas W. Wood
Grazia Devigili
Cécile Cauquil
Horvath, Rita [0000-0002-9841-170X]
Chinnery, Patrick [0000-0002-7065-6617]
Apollo - University of Cambridge Repository
Tozza, Stefano [0000-0002-9672-4577]
Rossor, Alexander M [0000-0003-4648-2896]
Horga, Alejandro [0000-0002-2120-2213]
Source :
Brain
Publication Year :
2019

Abstract

See Paisán-Ruiz and Jen (doi:10.1093/brain/awaa015) for a scientific commentary on this article. Cortese et al. describe the full disease phenotype, including progression of ataxia, in 100 confirmed carriers of RFC1 repeat expansions. RFC1 repeat expansion should be considered in all cases of sensory ataxic neuropathy, particularly if cerebellar dysfunction, vestibular involvement and cough coexist.<br />Ataxia, causing imbalance, dizziness and falls, is a leading cause of neurological disability. We have recently identified a biallelic intronic AAGGG repeat expansion in replication factor complex subunit 1 (RFC1) as the cause of cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS) and a major cause of late onset ataxia. Here we describe the full spectrum of the disease phenotype in our first 100 genetically confirmed carriers of biallelic repeat expansions in RFC1 and identify the sensory neuropathy as a common feature in all cases to date. All patients were Caucasian and half were sporadic. Patients typically reported progressive unsteadiness starting in the sixth decade. A dry spasmodic cough was also frequently associated and often preceded by decades the onset of walking difficulty. Sensory symptoms, oscillopsia, dysautonomia and dysarthria were also variably associated. The disease seems to follow a pattern of spatial progression from the early involvement of sensory neurons, to the later appearance of vestibular and cerebellar dysfunction. Half of the patients needed walking aids after 10 years of disease duration and a quarter were wheelchair dependent after 15 years. Overall, two-thirds of cases had full CANVAS. Sensory neuropathy was the only manifestation in 15 patients. Sixteen patients additionally showed cerebellar involvement, and six showed vestibular involvement. The disease is very likely to be underdiagnosed. Repeat expansion in RFC1 should be considered in all cases of sensory ataxic neuropathy, particularly, but not only, if cerebellar dysfunction, vestibular involvement and cough coexist.

Details

ISSN :
14602156
Volume :
143
Issue :
2
Database :
OpenAIRE
Journal :
Brain : a journal of neurology
Accession number :
edsair.doi.dedup.....06b621364d74ac06a1f4907a87bf4d5c