2006
DOI: 10.1111/j.1526-4610.2006.00504.x
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Migrainous Vertigo: Mutation Analysis of the Candidate Genes CACNA1A, ATP1A2, SCN1A, and CACNB4

Abstract: Based on this group of patients there is no evidence that the genes causing FHM and EA-2 represent major susceptibility loci for MV.

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Cited by 74 publications
(46 citation statements)
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“…Analyses of candidate genes, however, have been negative in VM so far. 38,39 This study provides a longitudinal assessment of clinical symptoms and vestibulo-cochlear function in VM based on previously validated diagnostic criteria. 17 Diagnostic certainty was increased by repeat neurotologic assessment to rule out other causes of vertigo that had become apparent during follow-up.…”
Section: Resultsmentioning
confidence: 99%
“…Analyses of candidate genes, however, have been negative in VM so far. 38,39 This study provides a longitudinal assessment of clinical symptoms and vestibulo-cochlear function in VM based on previously validated diagnostic criteria. 17 Diagnostic certainty was increased by repeat neurotologic assessment to rule out other causes of vertigo that had become apparent during follow-up.…”
Section: Resultsmentioning
confidence: 99%
“…We suspect that the stable characteristics of central ocular motor disturbances are due to the treatment effects of prophylactic migraine medication. Possible causes of VM are vasospasms within the vestibular and/or auditory labyrinth [14,15,16] and dysfunction of voltage-sensitive ion channels or neurotransmitters alone or in combination with spreading depression [5,17,18,19,20,21,22]. Just as the pathophysiological mechanisms underlying VM have not yet been unraveled, it is also unclear how migraine prophylactics influence the course of the disease.…”
Section: Discussionmentioning
confidence: 99%
“…Until now, CACNA1A mutations have not been reported in children with isolated BPV, but literature data are scarce. In adult patients suffering from recurrent vertigo, large population screenings have been carried out but sequencing of different genes coding for ion channels did not reveal any deleterious abnormalities (20)(21)(22).…”
Section: Discussionmentioning
confidence: 99%