Katekolaminerg polymorf ventrikulaer takykardi er en sjaelden arvelig hjertesygdom

Anders Gaarsdal Holst; Jacob Tfelt-Hansen; Morten S Olesen; Juliane Theilade; Bo G Winkel; Alex H Christensen; Henning Bundgaard; Stig Haunsø; Jesper Hastrup Svendsen

Katekolaminerg polymorf ventrikulaer takykardi er en sjaelden arvelig hjertesygdom

Translated title of the contribution: [Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease]

Anders Gaarsdal Holst, Jacob Tfelt-Hansen, Morten S Olesen, Juliane Theilade, Bo G Winkel, Alex H Christensen, Henning Bundgaard, Stig Haunsø, Jesper Hastrup Svendsen

Abstract

Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease, which can lead to life-threatening ventricular arrhythmias in patients with a structurally normal heart. The age of onset is usually between two and 12 years and the initial symptom is frequently syncope or cardiac arrest. The arrhythmias are usually triggered by exercise or emotional affection. The diagnosis is often made using exercise electrocardiogram, which typically triggers arrhythmias. The treatment consists of beta blockers, frequently in combination with implantation of a cardioverter-defibrillator.

Translated title of the contribution	[Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease]
Original language	Danish
Journal	Ugeskrift for Laeger
Volume	172
Issue number	31
Pages (from-to)	2140-4
Number of pages	5
ISSN	0041-5782
Publication status	Published - 2 Aug 2010

Cite this

@article{1dbdd3a3313e49a29de976fb9410615a,

title = "Katekolaminerg polymorf ventrikulaer takykardi er en sjaelden arvelig hjertesygdom",

abstract = "Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease, which can lead to life-threatening ventricular arrhythmias in patients with a structurally normal heart. The age of onset is usually between two and 12 years and the initial symptom is frequently syncope or cardiac arrest. The arrhythmias are usually triggered by exercise or emotional affection. The diagnosis is often made using exercise electrocardiogram, which typically triggers arrhythmias. The treatment consists of beta blockers, frequently in combination with implantation of a cardioverter-defibrillator.",

author = "Holst, {Anders Gaarsdal} and Jacob Tfelt-Hansen and Olesen, {Morten S} and Juliane Theilade and Winkel, {Bo G} and Christensen, {Alex H} and Henning Bundgaard and Stig Hauns{\o} and Svendsen, {Jesper Hastrup}",

year = "2010",

month = aug,

day = "2",

language = "Dansk",

volume = "172",

pages = "2140--4",

journal = "Ugeskrift for Laeger",

issn = "0041-5782",

publisher = "Almindelige Danske Laegeforening",

number = "31",

}

TY - JOUR

T1 - Katekolaminerg polymorf ventrikulaer takykardi er en sjaelden arvelig hjertesygdom

AU - Holst, Anders Gaarsdal

AU - Tfelt-Hansen, Jacob

AU - Olesen, Morten S

AU - Theilade, Juliane

AU - Winkel, Bo G

AU - Christensen, Alex H

AU - Bundgaard, Henning

AU - Haunsø, Stig

AU - Svendsen, Jesper Hastrup

PY - 2010/8/2

Y1 - 2010/8/2

N2 - Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease, which can lead to life-threatening ventricular arrhythmias in patients with a structurally normal heart. The age of onset is usually between two and 12 years and the initial symptom is frequently syncope or cardiac arrest. The arrhythmias are usually triggered by exercise or emotional affection. The diagnosis is often made using exercise electrocardiogram, which typically triggers arrhythmias. The treatment consists of beta blockers, frequently in combination with implantation of a cardioverter-defibrillator.

AB - Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease, which can lead to life-threatening ventricular arrhythmias in patients with a structurally normal heart. The age of onset is usually between two and 12 years and the initial symptom is frequently syncope or cardiac arrest. The arrhythmias are usually triggered by exercise or emotional affection. The diagnosis is often made using exercise electrocardiogram, which typically triggers arrhythmias. The treatment consists of beta blockers, frequently in combination with implantation of a cardioverter-defibrillator.

M3 - Tidsskriftartikel

SN - 0041-5782

VL - 172

SP - 2140

EP - 2144

JO - Ugeskrift for Laeger

JF - Ugeskrift for Laeger

IS - 31

ER -

Katekolaminerg polymorf ventrikulaer takykardi er en sjaelden arvelig hjertesygdom

Abstract

Fingerprint

Cite this