A 42-year-old lady survived an episode of near-drowning and she was subsequently diagnosed with a rare genetic disease, recently classified as long QT 7 syndrome, for which she received an implantable cardioverter defibrillator. The features of this syndrome are herein described
Long QT syndrome (LQTS) is a hereditary ion channelopathy resulting in prolonged cardiac repolarizat...
SummaryThe short QT syndrome, a recently discovered ion channel disorder, combines shortened repolar...
Congenital long QT-syndrome (LQTS) was diagnosed in three patients. The first patient, a 10-year-old...
A 42-year-old lady survived an episode of near-drowning and she was subsequently diagnosed with a ra...
Andersen-Tawil syndrome (ATS), a rare autosomal dominant disorder, is characterized by periodic para...
A 55-year-old woman developed acute myocardial infarction while grieving for the death of her pet. T...
The first case of a patient with periodic paralysis of muscles accompanied by ventricular arrhythmia...
We report a 37-year-old woman with an out-of-hospital cardiac arrest caused by ventricular fibrillat...
A case of a 16-year old adolescent is presented who was referred for investigation of a syncopal epi...
Long QT intervals in the ECG have long been associated with sudden cardiac death. The congenital lon...
Background—Swimming is a relatively genotype-specific arrhythmogenic trigger for type 1 long-QT synd...
SummaryThis case report describes a 54-year-old man presenting with loss of consciousness due to acq...
Long QT syndrome (LQTS) is a heart disorder characterized by a prolongation of the QT interval on EC...
Long QT syndrome is associated with lethal tachyarrhythmia that can lead to syncope, seizure, and su...
Forty per cent (40%) of sudden unexpected natural deaths in people under 35 years of age are associa...
Long QT syndrome (LQTS) is a hereditary ion channelopathy resulting in prolonged cardiac repolarizat...
SummaryThe short QT syndrome, a recently discovered ion channel disorder, combines shortened repolar...
Congenital long QT-syndrome (LQTS) was diagnosed in three patients. The first patient, a 10-year-old...
A 42-year-old lady survived an episode of near-drowning and she was subsequently diagnosed with a ra...
Andersen-Tawil syndrome (ATS), a rare autosomal dominant disorder, is characterized by periodic para...
A 55-year-old woman developed acute myocardial infarction while grieving for the death of her pet. T...
The first case of a patient with periodic paralysis of muscles accompanied by ventricular arrhythmia...
We report a 37-year-old woman with an out-of-hospital cardiac arrest caused by ventricular fibrillat...
A case of a 16-year old adolescent is presented who was referred for investigation of a syncopal epi...
Long QT intervals in the ECG have long been associated with sudden cardiac death. The congenital lon...
Background—Swimming is a relatively genotype-specific arrhythmogenic trigger for type 1 long-QT synd...
SummaryThis case report describes a 54-year-old man presenting with loss of consciousness due to acq...
Long QT syndrome (LQTS) is a heart disorder characterized by a prolongation of the QT interval on EC...
Long QT syndrome is associated with lethal tachyarrhythmia that can lead to syncope, seizure, and su...
Forty per cent (40%) of sudden unexpected natural deaths in people under 35 years of age are associa...
Long QT syndrome (LQTS) is a hereditary ion channelopathy resulting in prolonged cardiac repolarizat...
SummaryThe short QT syndrome, a recently discovered ion channel disorder, combines shortened repolar...
Congenital long QT-syndrome (LQTS) was diagnosed in three patients. The first patient, a 10-year-old...
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