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Pathogenic Insights and Search for Biomarkers in RFC1-ataxia/CANVAS

RecruitingNAAges 18 Years - 80 YearsAllCatholic University of the Sacred Heart
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In plain words

What the trial is, and whether it could suit you

CANVAS (Cerebellar Ataxia, Neuropathy, Vestibular Areflexia Syndrome), also referred to as RFC1-ataxia, is a recently molecularly characterized neurodegenerative disorder caused by a biallelic expansion of an AAGGG pentanucleotide repeat in intron 2 of the Replication Factor C subunit 1 (RFC1) gene. This adult-onset condition presents with a variable combination of cerebellar ataxia, peripheral neuropathy, and vestibular dysfunction. Currently, limited data are available regarding its natural history and the molecular mechanisms by which this dynamic mutation leads to neurodegeneration of selective neuronal populations. Given that recent literature identifies RFC1/CANVAS as a relatively common genetic cause of late-onset ataxia, elucidation of its underlying pathogenic mechanisms may offer insights into the molecular pathways implicated in more prevalent late-onset neurodegenerative di

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: * Molecular diagnosis of RFC1-ataxia * age \>18 years and \<80 years * ability to sign informed consent Exclusion Criteria: * Diagnosis of other degenerative and/or non-degenerative neurological diseases * Not signed informed consent
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What it tests

  • Assessment of markers of oxidative stress in peripheral blood samples
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Where

2 sites
Alma Mater Studiorum University of Bologna
Bologna, Italy
Department of Neuroscience
Roma, Italy
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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