Arı, HatemKoyuncu, FerudunAvcı, AhmetDemir, KenanAltunkeser, Bülent Behlül2020-03-262020-03-2620131110-2608https://dx.doi.org/10.1016/j.ehj.2013.03.003https://hdl.handle.net/20.500.12395/30107The Brugada Syndrome (BrS) is a heterogeneous genetic disease characterized by persistent or transient ST-segment elevation in the right precordial electrocardiography (ECG) leads and a high incidence of sudden death and life-threatening ventricular tachyarrhythmias in patients with structurally normal hearts. The syndrome generally manifests in men during adulthood. The ECG manifestations can be overt or concealed. We report a case of BrS whose type 1 ECG pattern during febrile state converted to type 2 ECG after alleviation of fever with atypical characteristics (78-year-old woman with monomorphic ventricular tachycardia on holter monitoring, a history of the sudden infant death of her child, and without inducible ventricular arrhythmia by programed ventricular stimulation [PVS]). © 2012 Egyptian Society of Cardiology. Production and hosting by Elsevier B.V.en10.1016/j.ehj.2013.03.003info:eu-repo/semantics/openAccessBrugada SyndromeElectrocardiographyFeverArticle653235238Q3