Brugada syndrome genetic testing: Difference between revisions

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==Other Diagnostic Studies==
==Other Diagnostic Studies==


Genetic testing may be helpful in the diagnosis of Brugada syndrome. Findings suggestive of/diagnostic of [disease name] include:
Genetic testing may be helpful in the diagnosis of Brugada syndrome. Findings suggestive of/diagnostic of [disease name] include:<ref name="NielsenHolst2013">{{cite journal|last1=Nielsen|first1=Morten W.|last2=Holst|first2=Anders G.|last3=Olesen|first3=Søren-Peter|last4=Olesen|first4=Morten S.|title=The genetic component of Brugada syndrome|journal=Frontiers in Physiology|volume=4|year=2013|issn=1664-042X|doi=10.3389/fphys.2013.00179}}</ref>


*[Finding 1]
*[Finding 1]

Revision as of 14:58, 11 December 2019

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Overview

Despite the association of the Brugada syndrome with the SCN5A genotype, there is unfortunately no association between the results of genetic testing and clinical prognosis. Genetic testing can be used to support the diagnosis of Brugada syndrome and to detect relatives at risk.[1]

Other Diagnostic Studies

Genetic testing may be helpful in the diagnosis of Brugada syndrome. Findings suggestive of/diagnostic of [disease name] include:[2]

  • [Finding 1]
  • [Finding 2]
  • [Finding 3]

References

  1. Antzelevitch C, Brugada P, Borggrefe M, Brugada J, Brugada R, Corrado D, Gussak I, LeMarec H, Nademanee K, Perez Riera AR, Shimizu W, Schulze-Bahr E, Tan H, Wilde A (2005). "Brugada syndrome: report of the second consensus conference". Heart Rhythm : the Official Journal of the Heart Rhythm Society. 2 (4): 429–40. PMID 15898165. Unknown parameter |month= ignored (help); |access-date= requires |url= (help)
  2. Nielsen, Morten W.; Holst, Anders G.; Olesen, Søren-Peter; Olesen, Morten S. (2013). "The genetic component of Brugada syndrome". Frontiers in Physiology. 4. doi:10.3389/fphys.2013.00179. ISSN 1664-042X.

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