Europace Advance Access originally published online on August 11, 2008
Europace 2008 10(10):1224-1225; doi:10.1093/europace/eun199
Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2008. For permissions please email: journals.permissions@oxfordjournals.org
EHRA EDUCATION COMMITTEE: EDUCATION IN EP
A family with abnormal electrocardiograms: part I
Ans C.P. Wiesfeld1,* and
Isabelle C. van Gelder1,2
1 Department of Cardiology, Thoraxcenter, University Medical Center Groningen, University of Groningen, PO Box 30.001, 9700 RB Groningen, The Netherlands;
2 Interuniversity Cardiology Institute Netherlands, Utrecht, The Netherlands
Manuscript submitted 13 June 2008. Accepted after revision 11 July 2008.
* Corresponding author. Tel +31 50 3616161; fax: +31 50 3614391. E-mail address: a.c.p.wiesfeld{at}thorax.umcg.nl
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Introduction
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A 40-year-old woman (Patient 1) had a broad complex tachycardia
with left bundle branch block morphology and right axis compatible
with ventricular tachycardia. Her electrocardiogram (ECG) was
abnormal (
Figure 1). An echocardiogram revealed a moderate
depressed left ventricular function, especially wall motion
disturbances in the inferoposterolateral part with an ejection
fraction of 40%. The right ventricle had mild segmental dilatation
and a right ventricular ejection fraction of 40%. The signal-averaged
ECG was normal. A brother died suddenly at the age of 45 years.
Because of the suspicion of the hereditary disease, her 21-year-old
son (Patient 2) agreed for cardiac evaluation. His ECG is presented
in
Figure 2. His echocardiogram, 24 h ambulatory monitoring
(only one ventricular premature beat), and exercise test were
within normal limits. A late potential was present during signal-averaged
ECG.
Cardiac evaluation was suggested to a 46-year-old sister (Patient
3) without physical complaints. Her ECG is presented in
Figure 3.
The echocardiogram showed a dilated left ventricle with depressed
function and an ejection fraction of 30%. A late potential was
present during signal-averaged ECG. Twenty-four-hour ambulatory
monitoring registered one triplet and 2500 ventricular premature
beats and 24 doublets. During exercise testing polymorphic ventricular
premature beats and doublets occurred. Her identical twin sister
(evaluated by co-worker H. Heidbuchel, University of Leuven,
Leuven, Belgium) had exactly the same ECG.
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Questions
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- What abnormalities are seen in the presented 12-lead electrocardiograms? Can these abnormalities be explained by the same disease?
- What additional investigations are possible in Patients 1, 2, and 3?
- What kind of (anti-arrhythmic) therapy is possible in Patients 1, 2, and 3?

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