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Leigh syndrome with atypical cerebellar lesions

dc.contributor.authorVeiga, M
dc.contributor.authorMarecos, C
dc.contributor.authorDuarte, S
dc.contributor.authorVieira, JP
dc.contributor.authorConceição, C
dc.date.accessioned2019-12-16T12:13:12Z
dc.date.available2019-12-16T12:13:12Z
dc.date.issued2019
dc.description.abstractLeigh Syndrome is a neurodegenerative disorder caused by mitochondrial dysfunction, with significant phenotypic and genetic heterogeneity. It usually presents in early life, with a severe prognosis. It can be caused by more than 75 different gene mutations, of nuclear and mitochondrial origin, involving all respiratory chain complexes, with less than 25% of Leigh syndrome having mitochondrial DNA mutations. The typical pathologic hallmarks are focal, bilateral, and symmetric lesions in the basal ganglia, thalamus, cerebellum, cerebral white matter and spinal cord gray matter, usually with T2WI and FLAIR hyperintensity. The basal ganglia and thalami frequently present with a pattern of cytotoxic edema. We present one case with clinical and analytical features consistent with Leigh Syndrome, with peculiar imaging features, showing dominant cerebellar edematous changes with unexpected petechial component suggestive of microangiopathy. To our knowledge, these features are unreported and suggest the existence of microvascular lesions. Based on the reported imaging findings, we propose that Leigh Syndrome should be added to the differential diagnosis of acute cerebellitis.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationeNeurologicalSci. 2019 Jun 28;16:100197.pt_PT
dc.identifier.doi10.1016/j.ensci.2019.100197pt_PT
dc.identifier.issn2405-6502
dc.identifier.urihttp://hdl.handle.net/10400.10/2351
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherElsevierpt_PT
dc.relation.publisherversionhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6614543/pdf/main.pdfpt_PT
dc.subjectLeigh diseasept_PT
dc.subjectMagnetic resonance imagingpt_PT
dc.titleLeigh syndrome with atypical cerebellar lesionspt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlaceAmsterdampt_PT
oaire.citation.titleeNeurologicalScipt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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