This case describes the prenatal diagnosis and integrated peripartum management of a foetus with 2:1 atrioventricular block and torsade de pointes due to congenital long QT syndrome. The unique issues related to the detection of intrauterine conduction abnormalities and ventricular arrhythmias, along with the immediate postnatal care, have been described as an interesting teaching case with successful outcome
Prenatal diagnosis of long QT syndrome: Implications for delivery room and neonatal managemen
Background: The synchronised depolarization and repolarisation of the atria and ventricles is achiev...
BACKGROUND: cardiac arrhythmias are commonly observed in the fetus, however, may have major conseque...
We report a case of a fetus presenting with bradycardia, intermittent atrioventricular (AV) block, v...
Long-QT syndrome is a rare, inherited cardiac channelopathy that is characterized by arrhythmia, syn...
The diagnosis of long QT syndrome (LQTS) in utero presents many challenges for clinicians, and there...
Congenital long QT syndrome (cLQTS) is a channelopathy characterized by ventricular repolarization d...
Congenital long QT syndrome (LQTS) is a primary genetic and electrical disorder that increases risk ...
BackgroundFetal arrhythmias characteristic of long QT syndrome (LQTS) include torsades de pointes (T...
PubMedID: 22441564Congenital long QT syndrome (LQTS) is an inherited disorder characterized by QT pr...
ObjectivesThis study sought to determine the relationship between long QT syndrome (LQTS) subtype (L...
Introduction: Temporary QT-interval prolongation following intracranial hemorrhage and hydrocephalus...
Cardiac arrhythmias are very frequent in fetuses and newborns. The prognosis depends on the nature o...
We report a case of fetal trisomy 18 with SCN5A R1193Q variant that presented with sinus bradycardia...
Cardiac arrhythmias are very frequent in fetuses and newborns. The prognosis depends on the nature o...
Prenatal diagnosis of long QT syndrome: Implications for delivery room and neonatal managemen
Background: The synchronised depolarization and repolarisation of the atria and ventricles is achiev...
BACKGROUND: cardiac arrhythmias are commonly observed in the fetus, however, may have major conseque...
We report a case of a fetus presenting with bradycardia, intermittent atrioventricular (AV) block, v...
Long-QT syndrome is a rare, inherited cardiac channelopathy that is characterized by arrhythmia, syn...
The diagnosis of long QT syndrome (LQTS) in utero presents many challenges for clinicians, and there...
Congenital long QT syndrome (cLQTS) is a channelopathy characterized by ventricular repolarization d...
Congenital long QT syndrome (LQTS) is a primary genetic and electrical disorder that increases risk ...
BackgroundFetal arrhythmias characteristic of long QT syndrome (LQTS) include torsades de pointes (T...
PubMedID: 22441564Congenital long QT syndrome (LQTS) is an inherited disorder characterized by QT pr...
ObjectivesThis study sought to determine the relationship between long QT syndrome (LQTS) subtype (L...
Introduction: Temporary QT-interval prolongation following intracranial hemorrhage and hydrocephalus...
Cardiac arrhythmias are very frequent in fetuses and newborns. The prognosis depends on the nature o...
We report a case of fetal trisomy 18 with SCN5A R1193Q variant that presented with sinus bradycardia...
Cardiac arrhythmias are very frequent in fetuses and newborns. The prognosis depends on the nature o...
Prenatal diagnosis of long QT syndrome: Implications for delivery room and neonatal managemen
Background: The synchronised depolarization and repolarisation of the atria and ventricles is achiev...
BACKGROUND: cardiac arrhythmias are commonly observed in the fetus, however, may have major conseque...