DESCRIPTION : We report a sequence of ECGs recorded in a 61-yearold man admitted to a primary care hospital for a persistent chest pain. The patient was diagnosed 3 years ago for an asymptomatic Brugada type 1 syndrome (SCN5A Gly752Arg variant) as illustrated by the coved ST-segment elevation in the right precordial leads followed by a negative T wave (Panel A). He did not show positive evidence of sudden death in his family history. Although, his father died at age 38 in a car accident in unclear circumstances. The first ECG recorded in the emergency department showed an inferior STEMI with ST-segment elevation in the inferior leads (DII, DIII, aVF), posterior extension as demonstrated by a marked ST-segment depression in V1-V2 partially m...
Brugada syndrome is a congenital channelopathy in cardiac ion transmembrane causing an alteration in...
We identified a patient with the Brugada syndrome and frequent episodes of the traumatic syncope. Th...
In 1992, Brugada syndrom was introduced as a new clinical entity linking typical but variable ST seg...
History of present illness: A 56-year-old male, with a history of hypertension, diabetes, and dysli...
Introduction. Brugada syndrome is an arrhythmogenic disease characterized by coved ST segment eleva...
Brugada Syndrome has a unique electrocardiographic pattern of downsloping ST-segment elevation in th...
Summary: Brugada syndrome (BS) is an arrhythmogenic ion channelopathy, which constitutes a distinct ...
Brugada syndrome (BrS) has been described as an arrhythmic disorder characterized by ST elevation wi...
In December 2011, a 39-year-old man resuscitated from out-of-hospital cardiac arrest caused by ventr...
Brugada syndrome is a heritable arrhythmia syndrome that is characterized by an electrocardiographic...
Brugada syndrome is a heritable arrhythmia syndrome that is characterized by an electrocardiographic...
The Brugada syndrome (BrS) is an electrical heart disease with complex inheritance (some cases with ...
The Brugada Syndrome (BrS) is a heterogeneous genetic disease characterized by persistent or transie...
The Brugada syndrome is an inherited channelopathy that alters the main transmembrane ion currents t...
Introduction: The major electrocardiographic feature of Brugada syndrome is a distinct ST-segment el...
Brugada syndrome is a congenital channelopathy in cardiac ion transmembrane causing an alteration in...
We identified a patient with the Brugada syndrome and frequent episodes of the traumatic syncope. Th...
In 1992, Brugada syndrom was introduced as a new clinical entity linking typical but variable ST seg...
History of present illness: A 56-year-old male, with a history of hypertension, diabetes, and dysli...
Introduction. Brugada syndrome is an arrhythmogenic disease characterized by coved ST segment eleva...
Brugada Syndrome has a unique electrocardiographic pattern of downsloping ST-segment elevation in th...
Summary: Brugada syndrome (BS) is an arrhythmogenic ion channelopathy, which constitutes a distinct ...
Brugada syndrome (BrS) has been described as an arrhythmic disorder characterized by ST elevation wi...
In December 2011, a 39-year-old man resuscitated from out-of-hospital cardiac arrest caused by ventr...
Brugada syndrome is a heritable arrhythmia syndrome that is characterized by an electrocardiographic...
Brugada syndrome is a heritable arrhythmia syndrome that is characterized by an electrocardiographic...
The Brugada syndrome (BrS) is an electrical heart disease with complex inheritance (some cases with ...
The Brugada Syndrome (BrS) is a heterogeneous genetic disease characterized by persistent or transie...
The Brugada syndrome is an inherited channelopathy that alters the main transmembrane ion currents t...
Introduction: The major electrocardiographic feature of Brugada syndrome is a distinct ST-segment el...
Brugada syndrome is a congenital channelopathy in cardiac ion transmembrane causing an alteration in...
We identified a patient with the Brugada syndrome and frequent episodes of the traumatic syncope. Th...
In 1992, Brugada syndrom was introduced as a new clinical entity linking typical but variable ST seg...