Evidence map›Paper›PMID 41772445›Full record

ArticleBMC cardiovascular disorders2026

Ebstein's anomaly with life-threatening arrhythmia: an unusual cardiovascular manifestation of Williams syndrome - a case report.

M E Schouw, T T Koopmann, N A Blom, J L Stöger, D Q C M Barge-Schaapveld, R Bökenkamp

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Article in BMC cardiovascular disorders, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

M E SchouwDepartment of Clinical Genetics, Leiden University Medical Center, Albinusdreef 2, Leiden, 2333 ZA, Netherlands.
T T KoopmannDepartment of Clinical Genetics, Leiden University Medical Center, Albinusdreef 2, Leiden, 2333 ZA, Netherlands.
N A BlomDepartment of Pediatric Cardiology, Leiden University Medical Center, Albinusdreef 2, Leiden, 2333 ZA, Netherlands.
J L StögerDepartment of Radiology, Leiden University Medical Center, Albinusdreef 2, Leiden, 2333 ZA, Netherlands.
D Q C M Barge-SchaapveldDepartment of Clinical Genetics, Leiden University Medical Center, Albinusdreef 2, Leiden, 2333 ZA, Netherlands.
R BökenkampDepartment of Pediatric Cardiology, Leiden University Medical Center, Albinusdreef 2, Leiden, 2333 ZA, Netherlands. r.bokenkamp@lumc.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWilliams syndrome (WS) is a rare genetic multisystem disorder that often affects the cardiovascular system. However, an association with Ebstein’s anomaly (EA) is extremely uncommon. Previously, only two such cases have been reported. Here, we present a third patient with concurrent WS and EA, manifesting with life-threatening ventricular arrhythmias. CASE PRESENTATION: Our case involves an 11-year-old boy, diagnosed prenatally with EA and 3-months postnatally with WS on the basis of a 7q11.23 deletion. Over the course of follow-up since birth, life-threatening ventricular arrhythmias occurred, originating from a likely fibrosed Purkinje system possibly related to elastin haploinsufficiency. The resulting out-of-hospital cardiac arrest warranted implantation of an implantable cardioverter-defibrillator and antiarrhythmic medication.

conclusionsVentricular arrhythmia and out-of-hospital cardiac arrest constitute an unusual clinical presentation that has not previously been reported in cases with concurrent WS and EA, but may be attributed to elastin haploinsufficiency. This potentially fatal complication underscores the importance of vigilant clinical surveillance in patients with comparable congenital heart defects. Our case report adds further evidence to the limited literature describing congenital cardiac anomalies and associated complications in patients with WS.

Indexed as

Arrhythmias, CardiacEbstein AnomalyTachycardia, VentricularWilliams SyndromeAnti-Arrhythmia AgentsChildDefibrillators, ImplantableElectric CountershockGenetic Predisposition to DiseaseHaploinsufficiencyHumansMalePhenotypeTreatment OutcomeAnti-Arrhythmia AgentsCase reportEbstein’s anomalyVentricular arrhythmiasWilliams syndrome

Identifiers

PMID41772445
PMCPMC13059330

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