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dc.contributor.authorChumpol Anamnarten_US
dc.contributor.authorDittapong Songsaengen_US
dc.contributor.authorSirisak Chanpraserten_US
dc.contributor.otherChulalongkorn Universityen_US
dc.contributor.otherUniversity of Washington, Seattleen_US
dc.contributor.otherFaculty of Medicine, Siriraj Hospital, Mahidol Universityen_US
dc.date.accessioned2020-01-27T09:48:50Z-
dc.date.available2020-01-27T09:48:50Z-
dc.date.issued2019-05-30en_US
dc.identifier.citationBMC Neurology. Vol.19, No.1 (2019)en_US
dc.identifier.issn14712377en_US
dc.identifier.other2-s2.0-85066506007en_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/51638-
dc.description.abstract© 2019 The Author(s). Background: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a hereditary arteriopathy associated with the NOTCH3 gene. Clinical manifestations include strokes, transient ischaemic events, psychiatric disturbances, dementia, and migraines. We report a case of a Thai man with a severe CADASIL phenotype who presented with recurrent seizures and acute ischaemic stroke and classic vascular risk factors. Case presentation: A 50-year-old man with a history of mood disorder and progressive cognitive decline for 20 years as well as well-controlled diabetes mellitus and hypertension presented with recurrent generalized seizures and acute right-sided weakness. An MRI of the brain showed acute infarction of the left pons, a large number of cerebral microbleeds throughout the brain and white matter abnormalities without classic anterior temporal lobe lesions. Molecular genetic testing identified a homozygous pathologic variant, c.1672C > T (p. Arg558Cys), in the NOTCH3 gene. The diagnosis of CADASIL was confirmed. His clinical symptoms deteriorated, and he died of tracheobronchitis with secretion obstruction. Conclusion: This case raises awareness of an uncommon cause of acute ischaemic stroke in patients with classic vascular risk factors and emphasizes the need for a complete evaluation in cases with unexpected clinical presentation or unexpected diagnostic study results.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85066506007&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleA large number of cerebral microbleeds in CADASIL patients presenting with recurrent seizures: A case reporten_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1186/s12883-019-1342-2en_US
dc.identifier.urlhttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85066506007&origin=inwarden_US
Appears in Collections:Scopus 2019

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