Cardiovascular genomics and sudden cardiac death in the young.
Full text not available from this repository.| Item Type: | Article |
|---|---|
| Status: | Published |
| Official URL: | https://doi.org/10.31128/AJGP-09-18-4715 |
| Journal or Publication Title: | Australian Journal of General Practice |
| Volume: | 48 |
| Number: | 3 |
| Page Range: | pp. 90-95 |
| Date: | 2019 |
| Divisions: | Molecular Cardiology |
| Depositing User: | General Admin |
| Identification Number: | 10.31128/AJGP-09-18-4715 |
| ISSN: | 2208794X |
| Date Deposited: | 05 Jan 2021 05:23 |
| Abstract: | Background: Sudden cardiac death (SCD) in the young is a rare but tragic consequence of a number of genetic cardiovascular disorders. The care of survivors of cardiac arrest and families affected by SCD seeks to prevent further SCD events through family screening. Objective: The aim of this article is to review the genetic basis of SCD in the young and outline the clinical aspects of caring for families affected by SCD. Discussion: Inherited cardiomyopathies and primary arrhythmia syndromes are important causes of SCD in young people. Over the past 30 years, there has been an explosion of knowledge regarding the underlying genetic mechanisms of these disorders and dramatic advances in genetic testing technologies. Family screening with thorough multidisciplinary clinical assessment and genetic testing allows for the initiation of preventive strategies in high-risk relatives and ultimately a reduction in SCD events. |
| Creators: | Creators Email Isbister, Julia UNSPECIFIED Semsarian, Christopher UNSPECIFIED |
| Last Modified: | 05 Jan 2021 05:23 |
| URI: | https://eprints.centenary.org.au/id/eprint/908 |
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