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For cerebellar ataxia, neuropathy, and vestibular areflexia syndrome (CANVAS), the recessive biallelic (AAGGG)\n exp<\/jats:sub>\n genotype was present in ~92% of cases. This study aimed to examine whether the pentanucleotide repeat (PNR) was related to multiple system atrophy (MSA), which shares a spectrum of symptoms with CANVAS.\n <\/jats:p>\n <\/jats:sec>\n \n Methods<\/jats:title>\n \n In this study, we screened the pathogenic (AAGGG)\n exp<\/jats:sub>\n repeat and 5 other PNRs in 104 Chinese sporadic adult\u2010onset ataxia of unknown aetiology (SAOA) patients, 282 MSA patients, and 203 unaffected individuals. Multiple molecular genetic tests were used, including long\u2010range polymerase chain reaction (PCR), repeat\u2010primed PCR (RP\u2010PCR), Sanger sequencing, and Southern blot. Comprehensive clinical assessments were conducted, including neurological examination, neuroimaging, nerve electrophysiology, and examination of vestibular function.\n <\/jats:p>\n <\/jats:sec>\n \n Results<\/jats:title>\n \n We identified biallelic (AAGGG)\n exp<\/jats:sub>\n in 1 SAOA patient and 3 MSA patients. Additionally, 1 MSA patient had the (AAGGG)\n exp<\/jats:sub>\n \/(AAAGG)\n exp<\/jats:sub>\n genotype with uncertain pathogenicity. We also described the carrier frequency for different PNRs in our cohorts. Furthermore, we summarized the distinct phenotypes of affected patients, suggesting that biallelic (AAGGG)\n exp<\/jats:sub>\n in\n RFC1<\/jats:italic>\n could be associated with MSA and should be screened routinely in the MSA diagnostic workflow.\n <\/jats:p>\n <\/jats:sec>\n \n Interpretation<\/jats:title>\n \n Our results expanded the clinical phenotypic spectrum of\n RFC1<\/jats:italic>\n \u2010related disorders and raised the possibility that MSA might share the same genetic background as CANVAS, which is crucial for re\u2010evaluating the current CANVAS and MSA diagnostic criteria. ANN NEUROL 2020;88:1132\u20131143\n <\/jats:p>\n <\/jats:sec>","DOI":"10.1002\/ana.25902","type":"journal-article","created":{"date-parts":[[2020,9,17]],"date-time":"2020-09-17T00:03:40Z","timestamp":1600301020000},"page":"1132-1143","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":63,"title":["Biallelic Intronic\n AAGGG<\/scp>\n Expansion of\n \n RFC1<\/i>\n <\/scp>\n is Related to Multiple System Atrophy"],"prefix":"10.1002","volume":"88","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-3192-309X","authenticated-orcid":false,"given":"Linlin","family":"Wan","sequence":"first","affiliation":[{"name":"Department of Neurology, Xiangya Hospital Central South University Changsha China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Zhao","family":"Chen","sequence":"additional","affiliation":[{"name":"Department of Neurology, Xiangya Hospital Central South University Changsha China"},{"name":"Key Laboratory of 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