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Ugeskr Laeger. 2010 Aug 2;172(31):2140-4.

[Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease].

[Article in Danish]

Author information

1
Københavns Universitet, Danmarks Nationale Grundforskningsfonds Center for Hjertearytmi, Rigshospitalet, Hjertecentret, Hjertemedicinsk Klinik B, Laboratorium for Molekylaer Kardiologi. anders@kanten.dk

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.

PMID:
20670590
[Indexed for MEDLINE]
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