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CANVAS: a late onset ataxia due to biallelic intronic AAGGG expansions
by
Houlden, Henry
, Galassi, Deforie Valentina
, Cortese, Andrea
, Dominik, Natalia
in
Ataxia
/ Balance
/ Cerebellar ataxia
/ Cerebellum
/ Neurology
/ Neuropathy
/ Phenotypes
/ Replication factor C
/ Sensory neurons
/ Vestibular system
2021
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CANVAS: a late onset ataxia due to biallelic intronic AAGGG expansions
by
Houlden, Henry
, Galassi, Deforie Valentina
, Cortese, Andrea
, Dominik, Natalia
in
Ataxia
/ Balance
/ Cerebellar ataxia
/ Cerebellum
/ Neurology
/ Neuropathy
/ Phenotypes
/ Replication factor C
/ Sensory neurons
/ Vestibular system
2021
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Do you wish to request the book?
CANVAS: a late onset ataxia due to biallelic intronic AAGGG expansions
by
Houlden, Henry
, Galassi, Deforie Valentina
, Cortese, Andrea
, Dominik, Natalia
in
Ataxia
/ Balance
/ Cerebellar ataxia
/ Cerebellum
/ Neurology
/ Neuropathy
/ Phenotypes
/ Replication factor C
/ Sensory neurons
/ Vestibular system
2021
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CANVAS: a late onset ataxia due to biallelic intronic AAGGG expansions
Journal Article
CANVAS: a late onset ataxia due to biallelic intronic AAGGG expansions
2021
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Overview
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.
Publisher
Springer Nature B.V
Subject
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