Kort QT-syndrom som arvelig sygdom
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Kort QT-syndrom som arvelig sygdom. / Møller, Daniel Vega; Hedley, Paula L; Olesen, Morten; Kanters, Jørgen; Svendsen, Jesper Hastrup; Christiansen, Michael.
In: Ugeskrift for Laeger, Vol. 173, No. 6, 2011, p. 420-424.Research output: Contribution to journal › Journal article › Research › peer-review
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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
VL - 173
SP - 420
EP - 424
JO - Ugeskrift for Laeger
JF - Ugeskrift for Laeger
SN - 0041-5782
IS - 6
ER -
ID: 32476068