Zurich Open Repository and Archive University of Zurich University Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 2010 Wolff-Parkinson-White syndrome in a child with recurrent seizures Poretti, A ; Balmer, C DOI: https://doi.org/10.1017/S1047951109991004 Posted at the Zurich Open Repository and Archive, University of Zurich ZORA URL: https://doi.org/10.5167/uzh-44441 Journal Article Published Version Originally published at: Poretti, A; Balmer, C (2010). Wolff-Parkinson-White syndrome in a child with recurrent seizures. Cardiology in the Young, 20(1):78-79. DOI: https://doi.org/10.1017/S1047951109991004 Cardiology in the Young (2010), 20: 78–79 r Cambridge University Press, 2010 doi:10.1017/S1047951109991004 Images in Congenital Cardiac Disease Wolff-Parkinson-White syndrome in a child with recurrent seizures Andrea Poretti,1 Christian Balmer2 1 Department of Neurology; 2Department of Cardiology, University Children’s Hospital of Zurich, Switzerland Keywords: MELAS; ventricular hypertrophy; epilepsy Received: 11 November 2008; Accepted: 9 August 2009; First published online 17 February 2010 A 7-YEAR-OLD BOY WAS OBSERVED TO HAVE A short PR interval on monitoring during anaesthesia for tonsillectomy. Subsequent twelve-lead electrocardiograms (Fig 1) showed Wolff-Parkinson-White syndrome with delta waves seen best in leads I, II, and V3–V5, and a broad QRS complex. This was confirmed by electrophysiologic study, during which a left lateral accessory pathway with rapid antegrade conduction, down to a cycle length of 170 milliseconds, was successfully catheter ablated (arrow). At the age of 12 years, the patient experienced the onset of headache, vomiting, impaired visual acuity, and recurrent focal seizures. Blood and cerebrospinal fluid lactate were increased at 5.6 millimoles per litres with a reference unit of 1.0–2.6 millimoles per litres and 3.7 millimoles per litres with a reference unit of 0.9–2.2 millimoles per litres, respectively. Electroencephalogram showed epileptic discharges on the left occipital region, while magnetic resonance imaging of the brain revealed localised T2-hyperintensity of the left occipital cortex and cerebellar atrophy. The echocardiogram (Fig 2) in the parasternal long (a) and short (b) axis views demonstrated, for the first time, concentric left ventricular hypertrophy (arrows). The left ventricular posterior wall measured 11 millimetres – the upper limit of normal was 8 millimetres – and the ventricular function was normal, without outflow obstruction. MELAS syndrome Correspondence to: Dr Andrea Poretti, Department of Neurology, University Children’s Hospital, Steinwiesstrasse 75, CH-8032 Zurich, Switzerland. Tel: 1141 44 266 73 30; Fax: 1141 44 266 71 63; E-mail: Andrea.Poretti@kispi.uzh.ch (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes) was suspected, and the diagnostic A3243G mutation in mitochondrial Figure 1. Figure 2. Vol. 20, No. 1 Poretti and Balmer: Wolff-Parkinson-White syndrome tRNA was identified with a mutation load of 57% in blood lymphocytes. MELAS syndrome is known to be associated with both hypertrophic cardiomyopathy and conductions abnormalities, presumably as the consequence of impairment of oxidative phosphorylation in tissues with high energy demands.1 Wolff-Parkinson-White Syndrome occurs at least four times more frequently in patients with MELAS syndrome than in the normal population that is, 13% versus 1.5 to 3.1%. Moreover, as illustrated by our case, cardiac arrhythmias may precede neurological manifestations by many months or years, and patients who experience conduction abnormalities may have an earlier onset of neurological 79 symptoms. In patients with Wolff-Parkinson-White Syndrome and neurological symptoms, the presence of a MELAS syndrome should be considered. Acknowledgements We thank Prof. Sabina Gallati, Division of Human Genetics, University Children’s Hospital of Berne, Switzerland, for performing mutation analysis. Reference 1. Sproule DM, Kaufmann P, Engelstad K, Starc TJ, Hordof AJ, De Vivo DC. Wolff-Parkinson-White syndrome in Patients with MELAS. Arch Neurol 2007; 64: 1625–1627.