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

  • Sarah J. Beecroft
  • , Andrea Cortese
  • , Roisin Sullivan
  • , Wai Yan Yau
  • , Zoe Dyer
  • , Teddy Y. Wu
  • , Eoin Mulroy
  • , Luciana Pelosi
  • , Miriam Rodrigues
  • , Rachael Taylor
  • , Stuart Mossman
  • , Ruth Leadbetter
  • , James Cleland
  • , Tim Anderson
  • , Gianina Ravenscroft
  • , Nigel G. Laing
  • , Henry Houlden
  • , Mary M. Reilly
  • , Richard H. Roxburgh

Research output: Contribution to journalArticlepeer-review

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Abstract

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.

Original languageEnglish
Pages (from-to)2673-2680
Number of pages8
JournalBrain: A Journal of Neurology
Volume143
Issue number9
DOIs
Publication statusPublished - 1 Sept 2020

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