| Literature DB >> 30076629 |
A Sebastian López-Chiriboga1, Christopher Klein1,2, Anastasia Zekeridou1, Andrew McKeon1,2, Divyanshu Dubey2, Eoin P Flanagan1, Vanda A Lennon1,2,3, Jan-Mendelt Tillema1, Elaine C Wirrell1, Marc C Patterson1, Avi Gadoth2, J Gregory Aaen4, J Nicholas Brenton5, Jonathan D Bui6, Amanda Moen7, Catherine Otten8, Amanda Piquet9, Sean J Pittock1,2.
Abstract
The clinical phenotype of leucine-rich glioma-inactivated protein 1 (LGI1) and contactin-associated proteinlike 2 (CASPR2) autoimmunity is well defined in adults. Data for children are limited (<10 cases). Among 13,319 pediatric patients serologically tested for autoimmune neurological disorders (2010-2017), 264 were seropositive for voltage-gated potassium channel-complex-IgG (radioimmunoprecipitation). Only 13 (4.9%) were positive by transfected cell-binding assay for LGI1-IgG (n = 7), CASPR2-IgG (n = 3), or both (n = 3). This is significantly less than in adults. Encephalopathy, seizures, and peripheral nerve hyperexcitability were common, as was coexisting autoimmunity. No faciobrachial dystonic seizures or cancers were identified. Functional neurologic disorders were frequently the initial diagnosis, and immunotherapy appeared beneficial. Ann Neurol 2018;84:473-480.Entities:
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Year: 2018 PMID: 30076629 DOI: 10.1002/ana.25310
Source DB: PubMed Journal: Ann Neurol ISSN: 0364-5134 Impact factor: 10.422