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October 7, 1999New England Journal of Medicine145 citations

Molecular Diagnosis of the Inherited Long-QT Syndrome in a Woman Who Died after Near-Drowning

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MAMichael J. AckermanDTDavid J. TesterCPCo-burn J. Porter

Structured PICO

P
Population
1 woman who died after near-drowning
I
Intervention
Molecular diagnosis (genetic testing) for inherited long-QT syndrome

Highlights the potential role of inherited long-QT syndrome and the utility of molecular autopsy in unexplained drowning or near-drowning fatalities.

Abstract

Drowning accounts for more accidental deaths in children and adolescents than all other causes except motor vehicle accidents.1–3 Many of these fatalities are attributed to lack of supervision, trauma, alcohol or drug use, or seizures. However, an appreciable number of drownings have no satisfactory explanation. In these situations, cardiac arrhythmias, particularly those associated with the long-QT syndrome, may be an important consideration. The long-QT syndrome comprises a group of genetically distinct arrhythmogenic cardiovascular disorders, each resulting from a mutation in one of five genes encoding cardiac ion channels or auxiliary ion-channel subunits: KVLQT1 (at the LQT1 locus), HERG (at . . .

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Cite This Study

Ackerman et al. (1999) studied this question.

synapsesocial.com/papers/6a1b4df06e13c4b6f1abb3c2https://doi.org/10.1056/nejm199910073411504
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