Contribution of inherited heart disease to sudden cardiac death in childhood

Pediatrics

Volumn 120, Issue 4, 2007, Pages

  Hofman, Nynke ^a   Tan, Hanno L ^a   Clur, Sally Ann ^a   Alders, Mariel ^a   Van Langen, Irene M ^a   Wilde, Arthur A M ^a,b  

^a UNIVERSITY OF AMSTERDAM   (Netherlands)

^b ACADEMIC MEDICAL CENTER   (Netherlands)

Author keywords

Arrhythmia; Children; Genetic counseling; Molecular genetics; Sudden cardiac death

Indexed keywords

ADOLESCENT; ARTICLE; AUTOPSY; CHILD; CHILDHOOD; CLINICAL ARTICLE; CONTROLLED STUDY; DNA DETERMINATION; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAPHY; EXERCISE TEST; FAMILY; FEMALE; GENETIC COUNSELING; HEART DISEASE; HUMAN; MALE; MUTATION; PRIORITY JOURNAL; RELATIVE; SUDDEN DEATH;

ADOLESCENT; ALGORITHMS; CARDIOPULMONARY RESUSCITATION; CHILD; DEATH, SUDDEN; DEATH, SUDDEN, CARDIAC; DNA MUTATIONAL ANALYSIS; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAPHY; EXERCISE TEST; FEMALE; GENETIC COUNSELING; GENETIC SCREENING; HEART DISEASES; HUMANS; MALE; PEDIGREE;

EID: 35148819135     PISSN: 00314005     EISSN: 02105721     Source Type: Journal    
DOI: 10.1542/peds.2006-3751     Document Type: Article

References (19)

1. Berger S, Kugler JD, Thomas JA, Friedberg DZ. Sudden cardiac death in children and adolescents: introduction and overview. Pediatr Clin North Am. 2004:51:1201-1209
2. Blair PS, Sidebotham P, Berry PJ, Evans M, Fleming PJ. Major epidemiological changes in sudden infant death syndrome: a 10-year population-based study in the UK. Lancet. 2006;367:314-319
3. Campbell RM, Berger S. Preventing pediatric sudden cardiac death: where do we start? Pediatrics. 2006;118:802-804
4. Tester DJ, Ackerman MJ. Sudden infant death syndrome: how significant are the cardiac channelopathies? Cardiovasc Res. 2005;67:388-396
5. Steinberger J, Lucas RV, Edwards JE, Titus JL. Causes of sudden unexpected cardiac death in the first two decades of life. Am J Cardiol. 1996;77:992-995
6. Liberthson RR. Sudden death from cardiac causes in children and young adults. N Engl J Med. 1996;334:1039-1044
7. Marron BJ, Shirani J, Poliac LC, Mathenge R, Roberts WC, Mueller FO. Sudden death in young competitive athletes: clinical, demographic, and pathological profiles. JAMA. 1996;276:199-204
8. Chugh, SS, Kelly KL, Titus JL. Sudden cardiac death with apparently normal heart. Circulation. 2000;102:649-645
9. Corrado D, Basso C, Thiene G. Sudden death in young people with apparently normal heart. Cardiovasc Res. 2001;150:399-408
10. Puranik R, Chow CK, Duflou JA, Kilborn MJ, McGuire MA. Sudden death in the young. Heart Rhythm. 2005;2:1277-1282
11. Behr E, Wood DA, Wright M, Syrris P, Sheppard MN, Casey A, Davies MJ, McKenna W. Cardiological assessment of first-degree relatives in sudden arrhythmic death syndrome. Lancet. 2003;362:1457-1459
12. Tan HL, Hofman N, van Langen IM, van der Wal AC, Wilde AAM. Sudden unexplained death: heritability and diagnostic yield of cardiological and genetic examination in surviving relatives. Circulation. 2005;112:207-213
13. Wren C. Screening children with a family history of sudden cardiac death. Heart. 2006;92:1001-1006
14. Maron BJ. Hypertrophic cardiomyopathy in childhood. Pediatr Clin North Am. 2004;51:1305-1346
15. Van Driest SL, Vasile VC, Ommen SR, et al. Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy. J Am Coll Cardiol. 2004;44:1903-1910
16. Lekanne Deprez RH, Muurling-Vlietman JJ, Hruda J, et al. Two cases of severe neonatal hypertrophic cardiomyopathy caused by compound heterozygous mutations in the MYBPC3 gene. J Med Genet. 2006;43:829-832
17. Richard P, Charron P, Carrier L, et al. Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy. Circulation. 2003;107:2171-2174
18. Moss AJ, Robinson JL, Gessman L, et al. Comparison of clinical and genetic variables of cardiac events associated with loud noise versus swimming among subjects with the long QT syndrome. Am J Cardiol. 1999;84:876-879
19. Tester DJ, Kopplin LJ, Creighton W, Burke AP, Ackerman MJ. Pathogenesis of unexplained drowning: new insights from a molecular autopsy. Mayo Clin Proc. 2005;80:596-600