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dc.contributor.authorSmith, Paul
dc.contributor.authorNg, Kalun
dc.contributor.authorKrishnan, Kailash
dc.date.accessioned2025-05-09T14:13:08Z
dc.date.available2025-05-09T14:13:08Z
dc.date.issued2021
dc.identifier.citationSmith, P., Ng, K. and Krishnan, K. (2021) 'Fahr's disease with an initial presentation of crescendo TIA', BMJ Case Reports, 14(6), 242837. doi: 10.1136/bcr-2021-242837 https://doi.org/10.1136/bcr-2021-242837.en_US
dc.identifier.issn1757-790X
dc.identifier.urihttp://hdl.handle.net/20.500.12904/19492
dc.description.abstractA 51-year-old man presented with vertigo, slurred speech and left facial droop. He had been previously diagnosed with transient ischaemic attack (TIA) and had a prior lacunar infarct. Imaging showed heavy symmetrical calcification in the globus pallidus, frontal white matter and cerebellar dentate nuclei/deep white matter. The imaging was pathognomonic for Fahr's disease and diagnosis was confirmed when other secondary causes of hypercalcemia were excluded. Fahr's disease is a rare, autosomal dominant, neurological condition characterised by primary brain calcification. Patients present with progressive neurological and psychiatric symptoms; commonly, Parkinsonian movement disorders, seizures, headaches, dysarthria, cognitive decline, psychosis and personality changes. There is an association with intracerebral ischaemic events. This case supports a growing body of anecdotal evidence of this association and is the first in which crescendo TIA may be the initial presentation of Fahr's disease. Referral for genetic counselling and symptomatic relief for neurological symptoms are the main management strategies.Copyright © BMJ Publishing Group Limited 2021.
dc.description.urihttps://doi.org/10.1136/bcr-2021-242837en_US
dc.language.isoenen_US
dc.subjectCase reporten_US
dc.subjectFahr's diseaseen_US
dc.subjectStrokeen_US
dc.subjectTransient ischaemic attacken_US
dc.titleFahr's disease with an initial presentation of crescendo TIAen_US
dc.typeArticleen_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US
rioxxterms.versionVoRen_US
rioxxterms.versionofrecord10.1136/bcr-2021-242837en_US
rioxxterms.typeJournal Article/Reviewen_US
refterms.dateFCD2025-05-09T14:13:09Z
refterms.versionFCDVoR
refterms.panelUnspecifieden_US
html.description.abstractA 51-year-old man presented with vertigo, slurred speech and left facial droop. He had been previously diagnosed with transient ischaemic attack (TIA) and had a prior lacunar infarct. Imaging showed heavy symmetrical calcification in the globus pallidus, frontal white matter and cerebellar dentate nuclei/deep white matter. The imaging was pathognomonic for Fahr's disease and diagnosis was confirmed when other secondary causes of hypercalcemia were excluded. Fahr's disease is a rare, autosomal dominant, neurological condition characterised by primary brain calcification. Patients present with progressive neurological and psychiatric symptoms; commonly, Parkinsonian movement disorders, seizures, headaches, dysarthria, cognitive decline, psychosis and personality changes. There is an association with intracerebral ischaemic events. This case supports a growing body of anecdotal evidence of this association and is the first in which crescendo TIA may be the initial presentation of Fahr's disease. Referral for genetic counselling and symptomatic relief for neurological symptoms are the main management strategies.Copyright © BMJ Publishing Group Limited 2021.en_US
rioxxterms.funder.project94a427429a5bcfef7dd04c33360d80cden_US


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