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Spontaneous remission without progression to limbic encephalitis in a patient with LGi1 seropositive faciobrachial dystonic seizure
Neurology Asia ; : 191-193, 2016.
Article Dans Anglais | WPRIM | ID: wpr-625253
ABSTRACT
Faciobrachial dystonic seizures are pathognomonic of leucine-rich glioma inactivated-1 (LGi1) antibody, non-paraneoplastic limbic encephalitis. Faciobrachial dystonic seizures usually precede limbic encephalitis by about a month. It is unknown whether, if untreated, faciobrachial dystonic seizures inevitably progress to limbic encephalitis. We present an LGi1 seropositive patient with a year’s history of faciobrachial dystonic seizures, who achieved remission spontaneously without immunotherapy or antiepileptic drug treatment, and did not develop evidence of limbic encephalitis over a three-year follow-up.
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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Encéphalite limbique langue: Anglais Texte intégral: Neurology Asia Année: 2016 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Encéphalite limbique langue: Anglais Texte intégral: Neurology Asia Année: 2016 Type: Article