{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,28]],"date-time":"2026-09-28T21:29:35Z","timestamp":1790630975326,"version":"4.1.0"},"reference-count":78,"publisher":"Cambridge University Press (CUP)","license":[{"start":{"date-parts":[[2024,12,2]],"date-time":"2024-12-02T00:00:00Z","timestamp":1733097600000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Can. J. Neurol. Sci."],"abstract":"<jats:title>ABSTRACT:<\/jats:title>\n\t  <jats:sec id=\"S0317167124003354_as1\">\n\t    <jats:title>Background:<\/jats:title>\n\t    <jats:p>There is limited information on rare spinocerebellar ataxia (SCA) variants, particularly in the Canadian population. This study aimed to describe the demographic and clinical features of uncommon SCA subtypes in Canada and compare them with international data.<\/jats:p>\n\t  <\/jats:sec>\n\t  <jats:sec id=\"S0317167124003354_as2\">\n\t    <jats:title>Methods:<\/jats:title>\n\t    <jats:p>We conducted a case series and literature review of adult patients with rare SCA subtypes, including SCA5, SCA7, SCA12, SCA14, SCA15, SCA28, SCA34, SCA35 and SCA36. Data were collected from medical centers in Ontario, Alberta and Quebec between January 2000 and February 2021.<\/jats:p>\n\t  <\/jats:sec>\n\t  <jats:sec id=\"S0317167124003354_as3\">\n\t    <jats:title>Results:<\/jats:title>\n\t    <jats:p>We analyzed 25 patients with rare SCA subtypes, with onset ages ranging from birth to 67 years. Infantile and juvenile-onset cases were observed in SCA5, SCA7, SCA14 and SCA34. Most patients presented with gait ataxia, with no significant differences across groups. Additional common features included saccadic abnormalities (22 of 25), dysarthria (19 of 25) and nystagmus (12 of 22, except in SCA7). Less common findings included dystonia (8 of 25), cognitive impairment (7 of 25), tremor (9 of 25) and parkinsonism (3 of 25).<\/jats:p>\n\t  <\/jats:sec>\n\t  <jats:sec id=\"S0317167124003354_as4\">\n\t    <jats:title>Conclusion:<\/jats:title>\n\t    <jats:p>Our study highlights the heterogeneity of rare SCA subtypes in Canada. Ongoing longitudinal analysis will improve the understanding, management and screening of these disorders.<\/jats:p>\n\t  <\/jats:sec>","DOI":"10.1017\/cjn.2024.335","type":"journal-article","created":{"date-parts":[[2024,12,2]],"date-time":"2024-12-02T09:52:53Z","timestamp":1733133173000},"page":"1-10","source":"Crossref","is-referenced-by-count":3,"title":["Rare Spinocerebellar Ataxia Types in Canada: A Case Series and Review of the Literature"],"prefix":"10.1017","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-2857-4511","authenticated-orcid":false,"given":"Sohaila","family":"Alshimemeri","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lamya","family":"Alsaghan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-0291-1452","authenticated-orcid":false,"given":"Danah 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