A Māori specific RFC1 pathogenic repeat configuration in CANVAS, likely due to a founder allele

Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome (CANVAS) is a recently recognized neurodegenerative disease with onset in mid- to late adulthood. The genetic basis for a large proportion of Caucasian patients was recently shown to be the biallelic expansion of a pentanu...

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Veröffentlicht in:Brain (London, England : 1878) England : 1878), 2020-09, Vol.143 (9), p.2673-2680
Hauptverfasser: Beecroft, Sarah J, Cortese, Andrea, Sullivan, Roisin, Yau, Wai Yan, Dyer, Zoe, Wu, Teddy Y, Mulroy, Eoin, Pelosi, Luciana, Rodrigues, Miriam, Taylor, Rachael, Mossman, Stuart, Leadbetter, Ruth, Cleland, James, Anderson, Tim, Ravenscroft, Gianina, Laing, Nigel G, Houlden, Henry, Reilly, Mary M, Roxburgh, Richard H
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container_end_page 2680
container_issue 9
container_start_page 2673
container_title Brain (London, England : 1878)
container_volume 143
creator Beecroft, Sarah J
Cortese, Andrea
Sullivan, Roisin
Yau, Wai Yan
Dyer, Zoe
Wu, Teddy Y
Mulroy, Eoin
Pelosi, Luciana
Rodrigues, Miriam
Taylor, Rachael
Mossman, Stuart
Leadbetter, Ruth
Cleland, James
Anderson, Tim
Ravenscroft, Gianina
Laing, Nigel G
Houlden, Henry
Reilly, Mary M
Roxburgh, Richard H
description Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome (CANVAS) is a recently recognized neurodegenerative disease with onset in mid- to late adulthood. The genetic basis for a large proportion of Caucasian patients was recently shown to be the biallelic expansion of a pentanucleotide (AAGGG)n repeat in RFC1. Here, we describe the first instance of CANVAS genetic testing in New Zealand Māori and Cook Island Māori individuals. We show a novel, possibly population-specific CANVAS configuration (AAAGG)10-25(AAGGG)exp, which was the cause of CANVAS in all patients. There were no apparent phenotypic differences compared with European CANVAS patients. Presence of a common disease haplotype among this cohort suggests this novel repeat expansion configuration is a founder effect in this population, which may indicate that CANVAS will be especially prevalent in this group. Haplotype dating estimated the most recent common ancestor at ∼1430 ce. We also show the same core haplotype as previously described, supporting a single origin of the CANVAS mutation.
doi_str_mv 10.1093/brain/awaa203
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ispartof Brain (London, England : 1878), 2020-09, Vol.143 (9), p.2673-2680
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source Oxford University Press Journals All Titles (1996-Current); MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Adult
Aged
Alleles
Bilateral Vestibulopathy - diagnosis
Bilateral Vestibulopathy - ethnology
Bilateral Vestibulopathy - genetics
Cerebellar Ataxia - diagnosis
Cerebellar Ataxia - ethnology
Cerebellar Ataxia - genetics
Cohort Studies
Female
Founder Effect
Humans
Male
Middle Aged
Pedigree
Replication Protein C - genetics
title A Māori specific RFC1 pathogenic repeat configuration in CANVAS, likely due to a founder allele
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