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dc.contributor.authorStamenova, S
dc.contributor.authorRedha, I
dc.contributor.authorSchmierer, K
dc.contributor.authorGarcia, ME
dc.date.accessioned2021-05-21T13:48:45Z
dc.date.available2020-12-29
dc.date.available2021-05-21T13:48:45Z
dc.date.issued2021-02
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/71981
dc.description.abstractA 31-year-old pregnant woman presented with headache, fever and left-sided focal motor seizures, which progressed to bilateral tonic-clonic seizures. Her medical history included Crohn's disease treated with azathioprine and adalimumab, which were discontinued when she became pregnant. Her cerebro-spinal fluid was entirely normal and viral PCR negative. Extensive testing for infectious, autoimmune or malignant causes of encephalitis were non-revealing. MRI head showed unilateral cortical FLAIR-hyperintensity which on interval scans was seen bilaterally. Anti-myelin-oligodendrocyte glycoprotein (MOG)-IgG was positive leading to a diagnosis of cortical FLAIR-hyperintense lesions in Anti-MOG-associated Encephalitis with seizures (FLAMES).en_US
dc.format.extent102729
dc.languageeng
dc.relation.ispartofMultiple Sclerosis and Related Disorders
dc.subjectEncephalitisen_US
dc.subjectMOGen_US
dc.subjectMagnetic resonance imagingen_US
dc.subjectMyelin oligodentrocyte glycoproteinen_US
dc.subjectPregnancy, FLAMESen_US
dc.titleFLAIR-hyperintense lesions in anti-MOG-associated encephalitis with seizures (FLAMES) unmasked by withdrawal of immunosuppression for Crohn's disease?en_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.msard.2020.102729
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/33418310en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume48en_US
dcterms.dateAccepted2020-12-29
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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