Contextualizing Genetics for Regional Heart Failure Care.

Iyngkaran, Pupalan and Thomas, Merlin C and Johnson, Renee and French, John and Ilton, Marcus and McDonald, Peter and Hare, David L and Fatkin, Diane (2016) Contextualizing Genetics for Regional Heart Failure Care. Current Cardiology Reviews, 12 (3). pp.231-42. ISSN 1875-6557 (PMC OA)

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Abstract

Congestive heart failure (CHF) is a chronic and often devastating cardiovascular disorder with no cure. There has been much advancement in the last two decades that has seen improvements in morbidity and mortality. Clinicians have also noted variations in the responses to therapies. More detailed observations also point to clusters of diseases, phenotypic groupings, unusual severity and the rates at which CHF occurs. Medical genetics is playing an increasingly important role in answering some of these observations. This developing field in many respects provides more information than is currently clinically applicable. This includes making sense of the established single gene mutations or uncommon private mutations. In this thematic series which discusses the many factors that could be relevant for CHF care, once established treatments are available in the communities; this section addresses a contextual role for medical genetics.

Item Type: Article
Additional Information: This article is available for free from the PMC website: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5011192/
Subjects: R Medicine > R Medicine (General)
Depositing User: Repository Administrator
Date Deposited: 19 Oct 2016 01:35
Last Modified: 15 Jan 2018 21:50
URI: https://eprints.victorchang.edu.au/id/eprint/503

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