Multiple System Atrophy-like Phenotype Accompanied by Prominent Weight Loss and Fatigue.

Movement Disorders Clinical PracticeVolume 10, Issue S3 p. S45-S47 CASE REPORT Multiple System Atrophy-like Phenotype Accompanied by Prominent Weight Loss and Fatigue Xinhui Chen MD, Xinhui Chen MD Department of Neurology, The Second Affiliated Hospital, Zhejiang University School of Medicine, Zhejiang, ChinaSearch for more papers by this authorZhidong Cen PhD, Zhidong Cen PhD Department of Neurology, The Second Affiliated Hospital, Zhejiang University School of Medicine, Zhejiang, ChinaSearch for more papers by this authorBo Wang MD, Bo Wang MD Department of Neurology, The Second Affiliated Hospital, Zhejiang University School of Medicine, Zhejiang, ChinaSearch for more papers by this authorPeng Liu MD, Peng Liu MD Department of Neurology, Taizhou Central Hospital (Taizhou University Hospital), Zhejiang, ChinaSearch for more papers by this authorWei Luo MD, PhD, Corresponding Author Wei Luo MD, PhD [email protected] orcid.org/0000-0001-6951-7698 Department of Neurology, The Second Affiliated Hospital, Zhejiang University School of Medicine, Zhejiang, China Correspondence to: Dr. Wei Luo, Department of Neurology, the Second Affiliated Hospital, Zhejiang University School of Medicine, 88 Jiefang Road, Hangzhou, Zhejiang 310009, China; E-mail: [email protected]Search for more papers by this author Xinhui Chen MD, Xinhui Chen MD Department of Neurology, The Second Affiliated Hospital, Zhejiang University School of Medicine, Zhejiang, ChinaSearch for more papers by this authorZhidong Cen PhD, Zhidong Cen PhD Department of Neurology, The Second Affiliated Hospital, Zhejiang University School of Medicine, Zhejiang, ChinaSearch for more papers by this authorBo Wang MD, Bo Wang MD Department of Neurology, The Second Affiliated Hospital, Zhejiang University School of Medicine, Zhejiang, ChinaSearch for more papers by this authorPeng Liu MD, Peng Liu MD Department of Neurology, Taizhou Central Hospital (Taizhou University Hospital), Zhejiang, ChinaSearch for more papers by this authorWei Luo MD, PhD, Corresponding Author Wei Luo MD, PhD [email protected] orcid.org/0000-0001-6951-7698 Department of Neurology, The Second Affiliated Hospital, Zhejiang University School of Medicine, Zhejiang, China Correspondence to: Dr. Wei Luo, Department of Neurology, the Second Affiliated Hospital, Zhejiang University School of Medicine, 88 Jiefang Road, Hangzhou, Zhejiang 310009, China; E-mail: [email protected]Search for more papers by this author First published: 24 August 2023 https://doi.org/10.1002/mdc3.13802Citations: 1Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. References 1Wenning GK, Stankovic I, Vignatelli L, et al. The Movement Disorder Society criteria for the diagnosis of multiple system atrophy. Mov Disord 2022; 37: 1131–1148. https://doi.org/10.1002/mds.29005 [published Online First: 2022/04/22]. 2Turk BR, Theda C, Fatemi A, Moser AB. X-linked adrenoleukodystrophy: pathology, pathophysiology, diagnostic testing, newborn screening and therapies. Int J Dev Neurosci 2020; 80(1): 52–72. https://doi.org/10.1002/jdn.10003 [published Online First: 2020/01/08]. 3Ogaki K, Koga S, Aoki N, et al. 2016, Adult-onset cerebello-brainstem dominant form of X-linked adrenoleukodystrophy presenting as multiple system atrophy: case report and literature review. 4Chen Y-H, Lee Y-C, Tsai Y-S, et al. Unmasking adrenoleukodystrophy in a cohort of cerebellar ataxia. PLoS One 2017; 12(5):e0177296. https://doi.org/10.1371/journal.pone.0177296 [published Online First: 2017/05/08]. 5Salsano E, Marotta G, Manfredi V, et al. Brain fluorodeoxyglucose PET in adrenoleukodystrophy. Neurology 2014; 83(11): 981–989. https://doi.org/10.1212/wnl.0000000000000770 [published Online First: 2014/08/08]. 6Rice CM, McGuone D, Kurian KM, Love S, Renowden SA, Giffin NJ. Autopsy-confirmed, co-existent CADASIL and multiple system atrophy. Parkinsonism Relat Disord 2011; 17(5): 390–392. https://doi.org/10.1016/j.parkreldis.2011.01.004 [published Online First: 2011/02/15]. 7Stamelou M, Quinn NP, Bhatia KP. “atypical” atypical parkinsonism: new genetic conditions presenting with features of progressive supranuclear palsy, corticobasal degeneration, or multiple system atrophy-a diagnostic guide. Mov Disord 2013; 28(9): 1184–1199. https://doi.org/10.1002/mds.25509 [published Online First: 2013/05/31]. Citing Literature Volume10, IssueS3Supplement: Cases from the 2022 International CongressAugust 2023Pages S45-S47 ReferencesRelatedInformation