Arrhythmia Phenotype During Fetal Life Suggests Long-QT Syndrome Genotype: Risk Stratification of Perinatal Long-QT Syndrome

BACKGROUND—Fetal arrhythmias characteristic of long QT syndrome (LQTS) include torsades de pointes (TdP) and/or 2° atrioventricular block, but sinus bradycardia, defined as fetal heart rate

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Circulation. Arrhythmia and electrophysiology 2013-10, Vol.6 (5), p.946-951
Hauptverfasser:	Cuneo, Bettina F, Etheridge, Susan P, Horigome, Hitoshi, Sallee, Denver, Moon-Grady, Anita, Weng, Hsin-Yi, Ackerman, Michael J, Benson, D Woodrow
Format:	Artikel
Sprache:	eng
Schlagworte:	Atrioventricular Block - diagnosis Atrioventricular Block - genetics Atrioventricular Block - physiopathology Bradycardia - diagnosis Bradycardia - genetics Bradycardia - physiopathology Echocardiography Electrocardiography ERG1 Potassium Channel Ether-A-Go-Go Potassium Channels - genetics Female Genetic Testing Genotype Heart Rate Humans Infant, Newborn KCNQ1 Potassium Channel - genetics Long QT Syndrome - diagnosis Long QT Syndrome - genetics Long QT Syndrome - physiopathology Mutation NAV1.5 Voltage-Gated Sodium Channel - genetics Phenotype Pregnancy Pregnancy Outcome Prenatal Diagnosis Risk Assessment
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Beschreibung
Zusammenfassung:	BACKGROUND—Fetal arrhythmias characteristic of long QT syndrome (LQTS) include torsades de pointes (TdP) and/or 2° atrioventricular block, but sinus bradycardia, defined as fetal heart rate
ISSN:	1941-3149 1941-3084
DOI:	10.1161/CIRCEP.113.000618