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Updated: Feb 14, 2026

Evaluation of Left Ventricular Structure and Function using 3D Echocardiography
Published on: October 28, 2020
A case of Lamin C gene-mutation with preserved systolic function and ventricular dysrrhythmia
1Princess Alexandra Hospital, Brisbane.
Insights
Lamin C deficiency can cause dangerous arrhythmias even with normal heart function. An implantable defibrillator successfully treated ventricular tachycardia in a patient with Lamin C deficiency and preserved ejection fraction.
Area of Science:
- Cardiology
- Genetics
- Molecular Biology
Background:
- Lamin A/C gene mutations are linked to cardiomyopathy, heart failure, and arrhythmias.
- Current guidelines recommend implantable defibrillators for sudden cardiac death prevention only in severe left ventricular dysfunction.
- Lamin C deficiency presents a specific genetic cause of cardiomyopathy.
Abstract:
Lamin A/C gene-related cardiomyopathy is associated with progressive heart failure and malignant arrhythmias. Current guidelines advise the use of implantable defibrillators to prevent arrhythmogenic sudden cardiac death only in situations where there is evidence of severe left ventricular dysfunction. We describe a case of a woman with genetically confirmed Lamin C deficiency with preserved left ventricular function in whom an implantable defibrillator was inserted and within a month of implantation was used to terminate symptomatic ventricular tachycardia.
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