{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,7]],"date-time":"2026-09-07T03:21:44Z","timestamp":1788751304281,"version":"build-2803163510"},"reference-count":6,"publisher":"BMJ","issue":"12","content-domain":{"domain":["bmj.com"],"crossmark-restriction":true},"short-container-title":["BMJ Case Rep"],"accepted":{"date-parts":[[2021,11,30]]},"published-print":{"date-parts":[[2021,12]]},"abstract":"<jats:p>Acquired vocal cord paralysis (VCP) is caused by dysfunction or injury of one or both recurrent laryngeal nerves. Here we report a 41-year-old man with spinocerebellar atrophy, autosomal recessive type 10 (SCAR10) due to an autosomal recessive mutation in the ANO10 gene, with VCP as the presenting symptom. He later developed ataxia and speech disturbance.<\/jats:p>","DOI":"10.1136\/bcr-2021-245484","type":"journal-article","created":{"date-parts":[[2021,12,30]],"date-time":"2021-12-30T08:37:23Z","timestamp":1640853443000},"page":"e245484","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":5,"title":["Vocal cord paralysis as a presenting sign of autosomal recessive spinocerebellar atrophy type 10"],"prefix":"10.1136","volume":"14","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-7303-6416","authenticated-orcid":false,"given":"David","family":"Vaughan","sequence":"first","affiliation":[{"name":"Neurology, Cork University Hospital, Cork, Ireland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Adrinda","family":"Affendi","sequence":"additional","affiliation":[{"name":"ORL-HNS, South Infirmary Victoria University Hospital, Cork, Ireland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Patrick","family":"Sheahan","sequence":"additional","affiliation":[{"name":"ORL-HNS, South Infirmary Victoria University Hospital, Cork, Ireland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Brian","family":"Sweeney","sequence":"additional","affiliation":[{"name":"Neurology, Cork University Hospital Group, Cork, Ireland"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"239","published-online":{"date-parts":[[2021,12,30]]},"reference":[{"key":"2025082722282300000_14.12.e245484.1","doi-asserted-by":"publisher","DOI":"10.1097\/00005537-199809000-00016"},{"key":"2025082722282300000_14.12.e245484.2","doi-asserted-by":"publisher","DOI":"10.1001\/archotol.131.12.1086"},{"key":"2025082722282300000_14.12.e245484.3","doi-asserted-by":"publisher","DOI":"10.1016\/j.ajhg.2010.10.015"},{"key":"2025082722282300000_14.12.e245484.4","doi-asserted-by":"crossref","first-page":"258","DOI":"10.1002\/mdc3.12396","article-title":"Anoctamin 10-related autosomal recessive cerebellar ataxia: comprehensive clinical phenotyping of an Irish sibship","volume":"4","author":"Bogdanova-Mihaylova","year":"2017","journal-title":"Mov Disord Clin Pract"},{"key":"2025082722282300000_14.12.e245484.5","doi-asserted-by":"publisher","DOI":"10.1007\/s00415-014-7476-7"},{"key":"2025082722282300000_14.12.e245484.6","doi-asserted-by":"crossref","first-page":"1305","DOI":"10.1001\/jamaneurol.2014.193","article-title":"Autosomal recessive cerebellar ataxia type 3 due to ANO10 mutations: delineation and genotype-phenotype correlation study","volume":"71","author":"Renaud","year":"2014","journal-title":"JAMA Neurol"}],"container-title":["BMJ Case Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/bcr-2021-245484","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,8,28]],"date-time":"2025-08-28T05:28:32Z","timestamp":1756358912000},"score":1,"resource":{"primary":{"URL":"https:\/\/casereports.bmj.com\/lookup\/doi\/10.1136\/bcr-2021-245484"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2021,12]]},"references-count":6,"journal-issue":{"issue":"12","published-online":{"date-parts":[[2021,12,30]]},"published-print":{"date-parts":[[2021,12]]}},"alternative-id":["10.1136\/bcr-2021-245484"],"URL":"https:\/\/doi.org\/10.1136\/bcr-2021-245484","relation":{},"ISSN":["1757-790X"],"issn-type":[{"value":"1757-790X","type":"electronic"}],"subject":[],"published":{"date-parts":[[2021,12]]}}}