Case report of heterotaxy syndrome with sinus node dysfunction and left ventricular hypertrabeculation: clinical and genetic insights
We present the case of a 41-year-old woman with left atrial isomerism, severe sinus node dysfunction, and left ventricular hypertrabeculation, who required implantation of a dual-chamber implantable cardioverter-defibrillator with left bundle branch area pacing. Her family history revealed multiple cases of heterotaxy and conduction disorders. Genetic testing identified a heterozygous interstitial duplication on chromosome 17q23.2 involving the MED13 gene, whose clinical significance has not yet been determined.
Authors
- N. Essack
- Edward Dababneh (ORCID: https://orcid.org/0009-0009-8947-2963)
- María Gabriela Matta (ORCID: https://orcid.org/0000-0002-9651-1109)
- P. Dhonde
- Vaseekaran Gopalapillai (ORCID: https://orcid.org/0009-0003-4428-8085)
Institutions
- Gold Coast Hospital (AU)
Publication Details
- Journal
- Archivos Peruanos de Cardiología y Cirugía Cardiovascular
- Published
- 2025-07-30
- DOI
- https://doi.org/10.47487/apcyccv.v6i3.496
- Primary Topic
- Congenital heart defects research
- Type
- article
- Field-Weighted Citation Impact
- 0.00