Autosomal recessive catecholamine- or exercise-induced polymorphic ventricular tachycardia: Clinical features and assignment of the disease gene to chromosome 1p13-21

Circulation

Volumn 103, Issue 23, 2001, Pages 2822-2827

  Lahat, Hadas ^a,b   Eldar, Michael ^b,e   Levy Nissenbaum, Etgar ^a   Bahan, Tangiz ^a   Friedman, Eitan ^a,b   Khoury, Asad ^c   Lorber, Avraham ^c   Kastner, Daniel L ^d   Goldman, Boleslaw ^a   Pras, Elon ^a  

^a GERTNER INSTITUTE FOR EPIDEMIOLOGY AND HEALTH POLICY RESEARCH   (Israel)

^b TEL AVIV UNIVERSITY   (Israel)

^c RAMBAM MEDICAL CENTER   (Israel)

^d NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES   (United States)

^e SHEBA MEDICAL CENTER   (Israel)

Author keywords

Death, sudden; Genetics; Mapping; Syncope; Tachycardia

Indexed keywords

BETA ADRENERGIC RECEPTOR BLOCKING AGENT; CARRIER PROTEIN; CATECHOLAMINE; DNA MARKER; ISOPRENALINE; POTASSIUM CHANNEL;

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BRADYCARDIA; CHROMOSOME 1P; CLINICAL ARTICLE; CLINICAL FEATURE; EXERCISE; FEMALE; GENE ASSIGNMENT; GENE MAPPING; GENE SEQUENCE; GENETIC LINKAGE; HEART VENTRICLE TACHYCARDIA; HUMAN; ISRAEL; MALE; PRIORITY JOURNAL; SCHOOL CHILD; SEIZURE; SUDDEN DEATH; SYNCOPE;

EID: 0035849570     PISSN: 00097322     EISSN: None     Source Type: Journal    
DOI: 10.1161/01.CIR.103.23.2822     Document Type: Article

References (17)

1. Polymorphic ventricular tachyarrhythmias in the absence of organic heart disease: Classification, differential diagnosis, and implication for therapy
2. Bidirectional tachycardia in a child: A study using His bundle electrography
3. Catecholamine-induced severe ventricular arrhythmias with Adams Stokes syndrome in children: Report of four cases
4. Catecholaminergic polymorphic ventricular tachycardia in children: A 7-year follow-up of 21 patients
5. Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts
6. Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia
7. Evidence of genetic heterogeneity in the long QT syndrome
8. Strategies for multilocus linkage analysis in humans
9. Gene structures and expression profiles of three human KCND (Kv4) potassium channels mediating A-type currents Ito and Isa
10. Genetic and molecular basis of cardiac arrhythmias: Impact on clinical management
11. Localization of the human Ror1 gene (NTRKR1) to chromosome 1p31-p32 by fluorescence in situ hybridization and somatic cell hybrid analysis
12. Identification of a specific role for the Na, K-ATPase alpha-2 isoform as a regulator of calcium in the heart
13. Alteration of alpha 1 Na+,K(+)-ATPase 86Rb+ influx by a single amino acid substitution
14. Localization of the A(3) adenosine receptor gene (ADORA3) to human chromosome 1p
15. A physiological role of the adenosine A3 receptor: Sustained cardioprotection