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Acute facial diplegia and hyperreflexia: A Guillain-Barré syndrome variant.
Susuki, K; Atsumi, M; Koga, M; Hirata, K; Yuki, N.
Affiliation
  • Susuki K; Department of Neurology, Dokkyo University School of Medicine, Tochigi, Osaka, Japan. ksusuki@dokkyomed.ac.jp
Neurology ; 62(5): 825-7, 2004 Mar 09.
Article in En | MEDLINE | ID: mdl-15007144
Two patients with acute facial diplegia and hyperreflexia are described. Both patients had serologic evidence of preceding Campylobacter jejuni infection and antiganglioside IgG antibodies as well as other laboratory and electrophysiologic findings suggesting Guillain-Barré syndrome (GBS). IV immunoglobulin produced recovery. Hyperreflexia does not necessarily exclude the diagnosis of a GBS variant. Antiganglioside antibodies can help with diagnosis in difficult cases.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Guillain-Barre Syndrome / Facial Nerve Diseases / Muscle Spasticity Limits: Adult / Female / Humans Language: En Journal: Neurology Year: 2004 Document type: Article Affiliation country: Japan Country of publication: United States
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Collection: 01-internacional Database: MEDLINE Main subject: Guillain-Barre Syndrome / Facial Nerve Diseases / Muscle Spasticity Limits: Adult / Female / Humans Language: En Journal: Neurology Year: 2004 Document type: Article Affiliation country: Japan Country of publication: United States