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Acute Bilateral Mydriasis and Abducens Nerve Palsy with anti-GQ1b Antibody / 대한소아신경학회지
Article in English | WPRIM (Western Pacific) | ID: wpr-23609
Responsible library: WPRO
ABSTRACT
Ophthalmoplegia without ataxia has various etiologies. An atypical Miller Fisher syndrome implies an ophthalmoplegia without ataxia, areflexia or both. The presence of anti-GQ1b antibody supports the diagnosis of an atypical Miller Fisher syndrome. A 4-year-old Russian girl visited our hospital because of acute bilateral abducens nerve palsy and mydriasis. Although the muscle power of extremities was normal and she didn't show an ataxia, the deep tendon reflex of both knees and ankles was absent. The results of nerve conduction study and cerebrospinal fluid analysis were normal. Magnetic resonance imaging (MRI) showed an enhancement of the bilateral abducens nerve. The anti-Gq1b antibody titer was elevated. The diagnosis of atypical Miller Fisher syndrome was made and a therapy with intravenous immunoglobulins led to the clinical recovery. We report a girl with atypical Miller Fisher syndrome with acute bilateral abducens nerve palsy and mydriasis, diagnosed by of anti-GQ1b antibody positivity.
Subject(s)

Full text: Available Database: WPRIM (Western Pacific) Main subject: Abducens Nerve / Reflex, Stretch / Ataxia / Magnetic Resonance Imaging / Mydriasis / Cerebrospinal Fluid / Ophthalmoplegia / Immunoglobulins, Intravenous / Miller Fisher Syndrome / Abducens Nerve Diseases Type of study: Diagnostic study Limits: Child, preschool / Female / Humans Language: English Journal: Journal of the Korean Child Neurology Society Year: 2014 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Main subject: Abducens Nerve / Reflex, Stretch / Ataxia / Magnetic Resonance Imaging / Mydriasis / Cerebrospinal Fluid / Ophthalmoplegia / Immunoglobulins, Intravenous / Miller Fisher Syndrome / Abducens Nerve Diseases Type of study: Diagnostic study Limits: Child, preschool / Female / Humans Language: English Journal: Journal of the Korean Child Neurology Society Year: 2014 Document type: Article
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