Genetic Testing in Inherited Heart Diseases

Genetic Testing in Inherited Heart Diseases.

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Item Type: Review
Status: Published
Official URL: https://doi.org/10.1016/j.hlc.2019.10.014
Journal or Publication Title: Heart, Lung and Circulation
Volume: 29
Number: 4
Page Range: pp. 505-511
Date: 2020
Divisions: Cardio Genomics
Depositing User: General Admin
Identification Number: 10.1016/j.hlc.2019.10.014
ISSN: 14439506
Date Deposited: 22 Dec 2020 03:47
Abstract:

Inherited heart diseases include numerous conditions, from the more prevalent hypertrophic cardiomyopathy (HCM) and familial hypercholesterolaemia (FH), to the comparatively less common inherited arrhythmia syndromes, such as long QT syndrome (LQTS), catecholaminergic polymorphic ventricular tachycardia (CPVT) and Brugada syndrome (BrS). Genetic testing has evolved rapidly over the last decade and is now considered a mainstream component of clinical management of inherited heart diseases. Cardiac manifestations can also be part of wider syndromes, and genetic testing can play a critical role in clarifying the underlying aetiological basis of disease in some cases. The greatest utility of a genetic diagnosis, however, comes from the ability to elucidate disease risk amongst asymptomatic at-risk family members. Given the nuances and challenges, cardiac genetic testing is best performed in a multidisciplinary specialised clinic with access to cardiac genetic counselling.

Creators:
Creators
Email
Ingles, Jodie
UNSPECIFIED
Macciocca, Ivan
UNSPECIFIED
Morales, Ana
UNSPECIFIED
Thomson, Kate
UNSPECIFIED
Last Modified: 05 Jan 2021 21:45
URI: https://eprints.centenary.org.au/id/eprint/878

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