| Literature DB >> 32910249 |
Natalia Dominik1, Valentina Galassi Deforie2, Andrea Cortese2,3, Henry Houlden4.
Abstract
The ataxias are a group of disorders that manifest with balance, movement, speech and visual problems. They can arise due to dysfunction of the cerebellum, the vestibular system and/or the sensory neurons. Genetic defects are a common cause of chronic ataxia, particularly common are repeat expansions in this group of conditions. Co-occurrence of cerebellar ataxia with neuropathy and vestibular areflexia syndrome has been termed CANVAS. Although CANVAS is a rare syndrome, on discovery of biallelic expansions in the second intron of replication factor C subunit 1 (RFC1) gene, we and others have found the phenotype is broad and RFC1 expansions are a common cause of late-onset progressive ataxia.We aim to provide a review and update on recent developments in CANVAS and populations, where the disorder has been reported. We have also optimised a protocol for RFC1 expansion screening which is described herein and expanded phenotype after analysing late-onset ataxia patients from around the world.Entities:
Keywords: CANVAS; Late-onset ataxia; RFC1; Repeat expansion; Southern blot
Mesh:
Substances:
Year: 2020 PMID: 32910249 PMCID: PMC7914193 DOI: 10.1007/s00415-020-10183-0
Source DB: PubMed Journal: J Neurol ISSN: 0340-5354 Impact factor: 4.849