Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Congenital long QT syndrome and 2:1 atrioventricular block: an optimistic outcome in the current era.

Heart rhythm - 1 Jun 2010

Aziz Peter F, Tanel Ronn E, Zelster Ilana J, Pass Robert H, Wieand Tammy S, Vetter Victoria L, Vogel R Lee, Shah Maully J

Abstract excerpt

BACKGROUND: Previous studies of patients with long QT syndrome (LQTS) and 2:1 atrioventricular block (AVB) have reported a mortality rate greater than 50% during infancy. OBJECTIVE: The purpose of this study was to determine the outcome of this high-risk population in the current era. METHODS: A retrospective study from four tertiary care pediatric centers assessed patients with congenital LQTS and 2:1 AVB from...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adrenergic beta-Antagonists
Share to Anti-Arrhythmia Agents

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Atrioventricular Block

Share to Defibrillators, Implantable

Share to Flecainide

Share to Propanolamines

Share to Propranolol

Share to Torsades de Pointes

Source

Identifiers

PMID: 20197117
DOI: 10.1016/j.hrthm.2010.02.035

Genes

KCNH2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Congenital long QT syndrome and 2:1 atrioventricular block: an optimistic outcome in the current era.PMID 20197117Read ↗

Long QT syndrome in children in the era of implantable defibrillators.Semantic proximity Read ↗

Follow-up of 316 molecularly defined pediatric long-QT syndrome patients: clinical course, treatments, and side effects.Semantic proximity Read ↗

Beta-blocker efficacy in high-risk patients with the congenital long-QT syndrome types 1 and 2: implications for patient management.Semantic proximity Read ↗

Long QT syndrome in neonates: conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations.Semantic proximity Read ↗

Phenotype of Children with QT Prolongation Identified Using an Institution-Wide QT Alert System.Semantic proximity Read ↗

Catecholaminergic polymorphic ventricular tachycardia in children: analysis of therapeutic strategies and outcomes from an international multicenter registry.Semantic proximity Read ↗

Long QT syndrome: diagnosis and management.Semantic proximity Read ↗

Acquired long QT syndrome and torsade de pointes.Semantic proximity Read ↗

Clinical characteristics and genetic background of congenital long-QT syndrome diagnosed in fetal, neonatal, and infantile life: a nationwide questionnaire survey in Japan.Semantic proximity Read ↗

Low incidence of cardiac events with beta-blocking therapy in children with long QT syndrome.Semantic proximity Read ↗

Long QT syndrome due to a novel mutation in SCN5A: treatment with ICD placement at 1 month and left cardiac sympathetic denervation at 3 months of age.Semantic proximity Read ↗

Medical Therapy for Long QT Syndrome.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.