Molecular autopsy in the sudden cardiac death of a young woman: A first Canadian report

被引:3
|
作者
Rutberg, Julie
Green, Martin S.
Gow, Robert M.
Geraghty, Michael T.
Honeywell, Christina
Ewen, John
Birnie, David H.
Tang, Anthony
Lemery, Robert
Gollob, Michael H.
机构
[1] Univ Ottawa, Inst Heart, Arrhythmia Res Lab, Ottawa, ON K1Y 4W7, Canada
[2] Univ Ottawa, Div Cardiol, Ottawa, ON, Canada
[3] Childrens Hosp Eastern Ontario, Ottawa, ON K1H 8L1, Canada
[4] Guelph Gen Hosp, Guelph, ON, Canada
关键词
arrhythmia; genetics; long QT syndrome; sudden; cardiac death;
D O I
10.1016/S0828-282X(07)70849-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Standard autopsy of young victims with sudden cardiac death commonly does not identify a specific pathological diagnosis. In such cases, sudden cardiac death may be secondary to a genetic condition predisposing the patient to ventricular arrhythmias. Failure to identify a genetic etiology for an unexpected sudden death may leave surviving family members at risk for a similar tragedy. The case of a 21-year-old woman who died suddenly while at rest is presented. Molecular genetic analysis of tissue retrieved from the regional coroner's office identified a novel missense mutation in the KCNH2 gene, a gene known to cause the long QT syndrome.
引用
收藏
页码:904 / 906
页数:3
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