Coincidental occurance of episodic ataxia and multiple sclerosis: a case report and review of the literature

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dc.contributor.authorBatum M.
dc.contributor.authorKısabay Ak A.
dc.contributor.authorÇetin G.
dc.contributor.authorÇelebi H.B.G.
dc.contributor.authorÇam S.
dc.contributor.authorMavioğlu H.
dc.date.accessioned2024-07-22T08:05:20Z
dc.date.available2024-07-22T08:05:20Z
dc.date.issued2022
dc.description.abstractIntroduction: Episodic ataxia is a clinical condition characterized by episodes of balance and coordination problems that last minutes to hours. It can be inherited or sporadic, and it can be seen sporadically in epilepsy, basilar migraine, multiple sclerosis, vertebrobasilar ischaemia, and labyrinth diseases. Methods: In this article, we present a case of a patient who had a coincidental occurrence of episodic ataxia type 2 (EA2) and multiple sclerosis (MS) Results: The patient who had a previously unidentified heterozygous mutation in the calcium voltage-gated channel subunit alpha 1 A gene (CACNA1A). Conclusion: There is no publication in the literature reporting the co-occurrence of MS and EA2. This combination may be coincidental in this patient, or it may be a relationship that has not yet been scientifically revealed. © 2020 Informa UK Limited, trading as Taylor & Francis Group.
dc.identifier.DOI-ID10.1080/00207454.2020.1835896
dc.identifier.issn00207454
dc.identifier.urihttp://akademikarsiv.cbu.edu.tr:4000/handle/123456789/13082
dc.language.isoEnglish
dc.publisherTaylor and Francis Ltd.
dc.subjectAtaxia
dc.subjectCalcium Channels
dc.subjectHumans
dc.subjectMigraine with Aura
dc.subjectMultiple Sclerosis
dc.subjectacetazolamide
dc.subjectcalcium voltage gated channel subunit alpha 1a
dc.subjectcarbamazepine
dc.subjectglatiramer
dc.subjectimmunoglobulin G
dc.subjectmethylprednisolone
dc.subjectoligoclonal band
dc.subjectunclassified drug
dc.subjectvalproic acid
dc.subjectvoltage gated calcium channel
dc.subjectcalcium channel
dc.subjectabdominal pain
dc.subjectArticle
dc.subjectataxia
dc.subjectataxic gait
dc.subjectblurred vision
dc.subjectcase report
dc.subjectcaudate nucleus
dc.subjectcerebrospinal fluid analysis
dc.subjectcervical spinal cord
dc.subjectclinical article
dc.subjectcorticosteroid therapy
dc.subjectdiplopia
dc.subjectdizziness
dc.subjectdrug dose reduction
dc.subjectdrug pulse therapy
dc.subjectdrug withdrawal
dc.subjectdysarthria
dc.subjectelectroencephalogram
dc.subjectelectroencephalography
dc.subjectepilepsy
dc.subjectepileptic discharge
dc.subjectepisodic ataxia type 2
dc.subjectexon
dc.subjectfaintness
dc.subjectfamily history
dc.subjectfebrile convulsion
dc.subjectfemale
dc.subjectfever
dc.subjectfocal epilepsy
dc.subjectfollow up
dc.subjectframeshift mutation
dc.subjectgaze paralysis
dc.subjectgene sequence
dc.subjecthead movement
dc.subjecthematuria
dc.subjecthemiparesis
dc.subjectheterozygote
dc.subjectHoffmann reflex
dc.subjecthot flush
dc.subjecthuman
dc.subjecthyporeflexia
dc.subjectintron
dc.subjectiron deficiency anemia
dc.subjectlearning disorder
dc.subjectlimb weakness
dc.subjectmesencephalon
dc.subjectmetabolic acidosis
dc.subjectmultiple sclerosis
dc.subjectnausea
dc.subjectnuclear magnetic resonance imaging
dc.subjectnystagmus
dc.subjectpaternal inheritance
dc.subjectperception disorder
dc.subjectseizure
dc.subjectslurred speech
dc.subjectspastic gait
dc.subjectspasticity
dc.subjectspeech disorder
dc.subjectstop codon
dc.subjectthoracic spinal cord
dc.subjectvertigo
dc.subjectvisual acuity
dc.subjectvisual evoked potential
dc.subjectvomiting
dc.subjectwhite matter
dc.subjectataxia
dc.subjectcomplication
dc.subjectgenetics
dc.subjectmigraine with aura
dc.subjectmultiple sclerosis
dc.titleCoincidental occurance of episodic ataxia and multiple sclerosis: a case report and review of the literature
dc.typeArticle

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