| Literature DB >> 17876385 |
Julie Rutberg1, Martin S Green, Robert M Gow, Michael T Geraghty, Christina Honeywell, John Ewen, David H Birnie, Anthony Tang, Robert Lemery, Michael H Gollob.
Abstract
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.Entities:
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Year: 2007 PMID: 17876385 PMCID: PMC2651371 DOI: 10.1016/s0828-282x(07)70849-8
Source DB: PubMed Journal: Can J Cardiol ISSN: 0828-282X Impact factor: 5.223