Add to ORKGIntroduction: Temporary QT-interval prolongation following intracranial hemorrhage and hydrocephalus has been repeatedly reported in adults. Case: We report a case of excessive QT prolongation with sudden bradycardia resulting in 2:1 atrioventricular conduction in a preterm infant most likely associated with a congenital hydrocephalus. Pathomechanisms are discussed. Conclusion: Congenital hydrocephalus predisposes to excessive QT prolongation in preterm infants
Prolongation of the QT interval is the cause of about 10% cases of sudden infant death syndrome (SID...
Background: Electrocardiographic and molecular studies have clarified an association between sudden ...
PubMedID: 22441564Congenital long QT syndrome (LQTS) is an inherited disorder characterized by QT pr...
Introduction: Temporary QT-interval prolongation following intracranial hemorrhage and hydrocephalus...
Introduction - Temporary QT-interval prolongation following intracranial hemorrhage and hydrocephalu...
There is limited information in the literature about sudden infant death syndrome (SIDS) and apparen...
Background.The survival rate for extremely low birth weight (ELBW) infants born preterm is on an inc...
The recognition of ventricular repolarization abnormalities in the newborn carries several and sign...
This case describes the prenatal diagnosis and integrated peripartum management of a foetus with 2:1...
An understanding of the electrocardiogram in the newborn requires specific knowledge of the cardiac ...
A case of a 16-year old adolescent is presented who was referred for investigation of a syncopal epi...
Congenital long QT syndrome (cLQTS) is a channelopathy characterized by ventricular repolarization d...
BACKGROUND: Cisapride is a possible cause of potentially life threatening QT prolongation. AIMS: We ...
Long QT intervals in the ECG have long been associated with sudden cardiac death. The congenital lon...
Long-QT syndrome is a rare, inherited cardiac channelopathy that is characterized by arrhythmia, syn...
Prolongation of the QT interval is the cause of about 10% cases of sudden infant death syndrome (SID...
Background: Electrocardiographic and molecular studies have clarified an association between sudden ...
PubMedID: 22441564Congenital long QT syndrome (LQTS) is an inherited disorder characterized by QT pr...
Introduction: Temporary QT-interval prolongation following intracranial hemorrhage and hydrocephalus...
Introduction - Temporary QT-interval prolongation following intracranial hemorrhage and hydrocephalu...
There is limited information in the literature about sudden infant death syndrome (SIDS) and apparen...
Background.The survival rate for extremely low birth weight (ELBW) infants born preterm is on an inc...
The recognition of ventricular repolarization abnormalities in the newborn carries several and sign...
This case describes the prenatal diagnosis and integrated peripartum management of a foetus with 2:1...
An understanding of the electrocardiogram in the newborn requires specific knowledge of the cardiac ...
A case of a 16-year old adolescent is presented who was referred for investigation of a syncopal epi...
Congenital long QT syndrome (cLQTS) is a channelopathy characterized by ventricular repolarization d...
BACKGROUND: Cisapride is a possible cause of potentially life threatening QT prolongation. AIMS: We ...
Long QT intervals in the ECG have long been associated with sudden cardiac death. The congenital lon...
Long-QT syndrome is a rare, inherited cardiac channelopathy that is characterized by arrhythmia, syn...
Prolongation of the QT interval is the cause of about 10% cases of sudden infant death syndrome (SID...
Background: Electrocardiographic and molecular studies have clarified an association between sudden ...
PubMedID: 22441564Congenital long QT syndrome (LQTS) is an inherited disorder characterized by QT pr...