Genomet i kardiologien

Henning Bundgaard; Birgitte Rode Diness; Jacob Tfelt-Hansen; Finn Lund Henriksen; Ole Eschen; Flemming Skovby; Ole Havndrup; Henrik Kjærulf Jensen; Anne Tybjærg-Hansen

Genomet i kardiologien

Henning Bundgaard, Birgitte Rode Diness, Jacob Tfelt-Hansen, Finn Lund Henriksen, Ole Eschen, Flemming Skovby, Ole Havndrup, Henrik Kjærulf Jensen, Anne Tybjærg-Hansen

Institut for Klinisk Medicin

Abstract

Several cardiac diseases are autosomal dominantly inherited. This includes cardiomyopathies, primary arrhythmias (channelopathies), dyslipidaemias, premature ischaemic heart diseases and diseases of the thoracic aorta. Sudden cardiac death in the young is also often due to one of the inherited cardiac diseases. Clinical and genetic cascade family screening of the relatives to patients with inherited cardiac diseases is now organized in a national network of centres of cardiology, sharing pedigrees, clinical and genetic information. This gives unique opportunities for offering focused prophylaxis in the group of high-risk relatives.

Originalsprog	Dansk
Artikelnummer	V06140376
Tidsskrift	Ugeskrift for Laeger
Vol/bind	176
Udgave nummer	46
Antal sider	5
ISSN	0041-5782
Status	Udgivet - 2014

Adgang til dokumentet

http://ugeskriftet.dk/videnskab/genomet-i-kardiologien

Citationsformater

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AU - Bundgaard, Henning

AU - Diness, Birgitte Rode

AU - Tfelt-Hansen, Jacob

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AU - Eschen, Ole

AU - Skovby, Flemming

AU - Havndrup, Ole

AU - Jensen, Henrik Kjærulf

AU - Tybjærg-Hansen, Anne

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AB - Several cardiac diseases are autosomal dominantly inherited. This includes cardiomyopathies, primary arrhythmias (channelopathies), dyslipidaemias, premature ischaemic heart diseases and diseases of the thoracic aorta. Sudden cardiac death in the young is also often due to one of the inherited cardiac diseases. Clinical and genetic cascade family screening of the relatives to patients with inherited cardiac diseases is now organized in a national network of centres of cardiology, sharing pedigrees, clinical and genetic information. This gives unique opportunities for offering focused prophylaxis in the group of high-risk relatives.

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