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dc.rights.licenseopenen_US
dc.contributor.authorBERSANO, A.
dc.contributor.authorKRAEMER, M.
dc.contributor.authorBURLINA, A.
dc.contributor.authorMANCUSO, M.
dc.contributor.authorFINSTERER, J.
dc.contributor.authorSACCO, S.
dc.contributor.authorSALVARANI, C.
dc.contributor.authorCAPUTI, L.
dc.contributor.authorCHABRIAT, H.
dc.contributor.authorOBERSTEIN, S. L.
dc.contributor.authorFEDERICO, A.
dc.contributor.authorLASSERVE, E. T.
dc.contributor.authorHUNT, D.
dc.contributor.authorDICHGANS, M.
dc.contributor.authorARNOLD, M.
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorDEBETTE, Stephanie
dc.contributor.authorMARKUS, H. S.
dc.date.accessioned2021-08-26T10:07:16Z
dc.date.available2021-08-26T10:07:16Z
dc.date.issued2021-08
dc.identifier.issn1432-1459 (Electronic) 0340-5354 (Linking)en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/110218
dc.description.abstractEnDespite intensive investigations, about 30% of stroke cases remains of undetermined origin. After exclusion of common causes of stroke, there is a number of rare heritable and non-heritable conditions, which often remain misdiagnosed, that should be additionally considered in the diagnosis of cryptogenic stroke. The identification of these diseases requires a complex work up including detailed clinical evaluation for the detection of systemic symptoms and signs, an adequate neuroimaging assessment and a careful family history collection. The task becomes more complicated by phenotype heterogeneity since stroke could be the primary or unique manifestation of a syndrome or represent just a manifestation (sometimes minor) of a multisystem disorder. The aim of this review paper is to provide clinicians with an update on clinical and neuroradiological features and a set of practical suggestions for the diagnostic work up and management of these uncommon causes of stroke. The identification of these stroke causes is important to avoid inappropriate and expensive diagnostic tests, to establish appropriate management measures, including presymptomatic testing, genetic counseling, and, if available, therapy. Therefore, physicians should become familiar with these diseases to provide future risk assessment and family counseling.
dc.language.isoENen_US
dc.subject.enRare strokes
dc.subject.enMonogenic diseases
dc.subject.enCADASIL
dc.subject.enCARASIL
dc.subject.enFabry disease
dc.subject.enCOL4A1 syndrome
dc.subject.enRetinal vasculopathy with cerebral leukoencephalopathy
dc.subject.enMELAS
dc.subject.enCARASAL
dc.subject.enSneddon syndrome
dc.subject.enSusac syndrome
dc.subject.enPrimary angiitis of the central nervous system
dc.subject.enMoyamoya angiopathy
dc.subject.enTakotsubo syndrome
dc.subject.enReversible Cerebral Vasoconstriction Syndrome
dc.title.enHeritable and non-heritable uncommon causes of stroke
dc.typeArticle de revueen_US
dc.identifier.doi10.1007/s00415-020-09836-xen_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed32318851en_US
bordeaux.journalJournal of Neurologyen_US
bordeaux.page2780-2807en_US
bordeaux.volume268en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.issue8en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamVINTAGEen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03326650
hal.version1
hal.date.transferred2021-08-26T10:07:19Z
hal.exporttrue
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