{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,2]],"date-time":"2026-10-02T04:15:56Z","timestamp":1790914556722,"version":"4.1.0"},"reference-count":21,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2015,6,15]],"date-time":"2015-06-15T00:00:00Z","timestamp":1434326400000},"content-version":"vor","delay-in-days":106,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"name":"Kangdong Sacred Heart Hospital Fund","award":["2014-14"],"award-info":[{"award-number":["2014-14"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Peripheral Nervous Sys"],"published-print":{"date-parts":[[2015,3]]},"abstract":"Abstract<\/jats:title>A variant of Guillain\u2010Barr\u00e9 syndrome (GBS<\/jats:styled-content>) with predominant manifestation of facial diplegia (FD<\/jats:styled-content>) has been described recently. This study aimed to characterize and determine the incidence of this FD<\/jats:styled-content>\u2010predominant GBS<\/jats:styled-content> variant. The clinical and serological information of 900 consecutive patients were reviewed. In total, eight patients were identified between January 2007 and December 2010 as having FD<\/jats:styled-content> accompanied by some features of GBS<\/jats:styled-content>. These features were subjective sensory symptoms such as distal paresthesia (7\/8, 88%), albumin\u2010cytological (A\/C) dissociation (7\/8, 88%), antecedent infection (6\/8, 75%), and minor nerve conduction study (NCS<\/jats:styled-content>) abnormalities (5\/7, 71%). One patient presented with the typical NCS<\/jats:styled-content> feature of demyelinating neuropathy. Only two patients exhibited areflexia (2\/8, 25%). None of the patients possessed any anti\u2010ganglioside antibodies; however, the serum of two patients was positive for anti\u2010mycoplasma antibody (2\/6, 33%). FD<\/jats:styled-content> variant of GBS<\/jats:styled-content> occurred in less than 1% of our dataset. FD<\/jats:styled-content> can be a regional variant of GBS<\/jats:styled-content> when it is accompanied by supporting features, such as subjective tingling, A\/C dissociation, and minor NCS<\/jats:styled-content> abnormalities.<\/jats:p>","DOI":"10.1111\/jns.12115","type":"journal-article","created":{"date-parts":[[2015,5,15]],"date-time":"2015-05-15T11:49:43Z","timestamp":1431690583000},"page":"32-36","source":"Crossref","is-referenced-by-count":21,"title":["When is facial diplegia regarded as a variant of Guillain\u2010Barr\u00e9 syndrome?"],"prefix":"10.1111","volume":"20","author":[{"given":"J. K.","family":"Kim","sequence":"first","affiliation":[{"name":"Department of Neurology Dong\u2010A University College of Medicine Busan Korea"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S. Y.","family":"Oh","sequence":"additional","affiliation":[{"name":"Department of Neurology Chonbuk National University College of Medicine Jeonju Korea"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"E. H.","family":"Sohn","sequence":"additional","affiliation":[{"name":"Department of Neurology Chungnam National University College of Medicine Daejeon Korea"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Y. H.","family":"Hong","sequence":"additional","affiliation":[{"name":"Department of Neurology Seoul National University Boramae Hospital Seoul Korea"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S. M.","family":"Jun","sequence":"additional","affiliation":[{"name":"Department of Neurology Dong\u2010A University College of Medicine Busan Korea"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J. 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