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Late-onset severe long QT syndrome.


ABSTRACT: We report a case of torsades de pointes arrhythmia as the first manifestation of congenital Long QT syndrome in a 77-year-old man with family history of sudden unexplained death. This case illustrates the importance of vigilant clinical assessment and genetic counseling in families with sudden death in order to identify properly asymptomatic relatives at risk for cardiac events. It also demonstrates that Long QT syndrome can still manifest with potentially fatal arrhythmias late in life in previously asymptomatic elderly patients.

SUBMITTER: Asatryan B 

PROVIDER: S-EPMC6931632 | biostudies-literature | 2018 Jul

REPOSITORIES: biostudies-literature

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Late-onset severe long QT syndrome.

Asatryan Babken B   Schaller André A   Bartholdi Deborah D   Medeiros-Domingo Argelia A  

Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc 20171130 4


We report a case of torsades de pointes arrhythmia as the first manifestation of congenital Long QT syndrome in a 77-year-old man with family history of sudden unexplained death. This case illustrates the importance of vigilant clinical assessment and genetic counseling in families with sudden death in order to identify properly asymptomatic relatives at risk for cardiac events. It also demonstrates that Long QT syndrome can still manifest with potentially fatal arrhythmias late in life in previ  ...[more]

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