Kort QT-syndrom som arvelig sygdom

Daniel Vega Møller; Paula L Hedley; Morten Olesen; Jørgen Kanters; Jesper Hastrup Svendsen; Michael Christiansen

Kort QT-syndrom som arvelig sygdom

Daniel Vega Møller, Paula L Hedley, Morten Olesen, Jørgen Kanters, Jesper Hastrup Svendsen, Michael Christiansen

1 Citationer (Scopus)

Abstract

Inherited ion-channel disorders can lead to life-threatening cardiac arrhythmias. A recent, rare entity has been discovered and termed short QT syndrome due to its electrocardiac features in conjunction with atrial and ventricular tachyarrhythmias as well as syncope and sudden cardiac death. The basis of the new syndrome is genetic and this review covers the genes responsible for the condition as well as the pathophysiology and diagnostic challenges involved in the syndrome. Furthermore, treatment for this new arrhythmic syndrome is reviewed.

Bidragets oversatte titel	[Short QT syndrome as an inherited condition]
Originalsprog	Dansk
Tidsskrift	Ugeskrift for Laeger
Vol/bind	173
Udgave nummer	6
Sider (fra-til)	420-424
Antal sider	5
Status	Udgivet - 2011

Citationsformater

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abstract = "Inherited ion-channel disorders can lead to life-threatening cardiac arrhythmias. A recent, rare entity has been discovered and termed short QT syndrome due to its electrocardiac features in conjunction with atrial and ventricular tachyarrhythmias as well as syncope and sudden cardiac death. The basis of the new syndrome is genetic and this review covers the genes responsible for the condition as well as the pathophysiology and diagnostic challenges involved in the syndrome. Furthermore, treatment for this new arrhythmic syndrome is reviewed.",

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year = "2011",

language = "Dansk",

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TY - JOUR

T1 - Kort QT-syndrom som arvelig sygdom

AU - Møller, Daniel Vega

AU - Hedley, Paula L

AU - Olesen, Morten

AU - Kanters, Jørgen

AU - Svendsen, Jesper Hastrup

AU - Christiansen, Michael

PY - 2011

Y1 - 2011

N2 - Inherited ion-channel disorders can lead to life-threatening cardiac arrhythmias. A recent, rare entity has been discovered and termed short QT syndrome due to its electrocardiac features in conjunction with atrial and ventricular tachyarrhythmias as well as syncope and sudden cardiac death. The basis of the new syndrome is genetic and this review covers the genes responsible for the condition as well as the pathophysiology and diagnostic challenges involved in the syndrome. Furthermore, treatment for this new arrhythmic syndrome is reviewed.

AB - Inherited ion-channel disorders can lead to life-threatening cardiac arrhythmias. A recent, rare entity has been discovered and termed short QT syndrome due to its electrocardiac features in conjunction with atrial and ventricular tachyarrhythmias as well as syncope and sudden cardiac death. The basis of the new syndrome is genetic and this review covers the genes responsible for the condition as well as the pathophysiology and diagnostic challenges involved in the syndrome. Furthermore, treatment for this new arrhythmic syndrome is reviewed.

M3 - Tidsskriftartikel

C2 - 21299935

SN - 0041-5782

VL - 173

SP - 420

EP - 424

JO - Ugeskrift for Laeger

JF - Ugeskrift for Laeger

IS - 6

ER -

Kort QT-syndrom som arvelig sygdom

Abstract

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Citationsformater