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Case Reports
. 2019 Feb;19(1):56-61.
doi: 10.1136/practneurol-2018-001959. Epub 2018 Oct 15.

Long QT syndrome masquerading as epilepsy

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Case Reports

Long QT syndrome masquerading as epilepsy

Clare M Galtrey et al. Pract Neurol. 2019 Feb.

Abstract

The diagnosis of epilepsy is incorrect in up to 20% of cases so should be revisited if attacks are not responding to treatment. We present a case of long QT syndrome that remained undiagnosed in the epilepsy clinic for 15 years until a near-fatal arrhythmia revealed the diagnosis and allowed effective treatment of her attacks. We hope this near miss raises awareness of long QT syndrome as a potentially fatal, rare but treatable condition that neurologists must consider in people with a label of refractory epilepsy. We provide practical pointers to increase the chance of early diagnosis and explore the impact of a late diagnosis for the patient and her family.

Keywords: anticonvulsants; cardiology; channels; epilepsy.

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Conflict of interest statement

Competing interests: None declared.

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