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Clinical manifestations of patients with CASPR2 antibodies

Authors
Sunwoo, Jun-SangLee, Soon-TaeByun, Jung-IckMoon, JangsupShin, Jung-WonJeong, Da-EunLee, Gun-HeeJeong, Seong HoShin, Yong-WonJung, Keun-HwaLee, Doo YoungJeon, DaejongJung, Ki-YoungKim, ManhoLee, Sang KunChu, Kon
Issue Date
Apr-2015
Publisher
ELSEVIER
Keywords
CASPR2; Epilepsy; Immunotherapy; Neuromyotonia
Citation
JOURNAL OF NEUROIMMUNOLOGY, v.281, pp 17 - 22
Pages
6
Journal Title
JOURNAL OF NEUROIMMUNOLOGY
Volume
281
Start Page
17
End Page
22
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/64610
DOI
10.1016/j.jneuroim.2015.03.005
ISSN
0165-5728
1872-8421
Abstract
Contactin-associated protein-like 2 (CASPR2) is one of the target antigens of voltage-gated potassium channels (VGKC) complex antibodies. There has been relatively little information in the literature regarding CASPR2 auto-immunity, especially in Asian population. We investigated the presence of CASPR2 antibodies in patients with presumed autoimmune neurological disorders and described the clinical features, laboratory findings, and responses to immunotherapy. Five patients were identified to be positive for CASPR2 antibodies. The results obtained here suggested that CASPR2 antibodies might be the possible cause of epilepsy even in the absence of typical features of limbic encephalitis and that immunotherapy could provide a favorable outcome. (C) 2015 Elsevier B.V. All rights reserved.
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