Related Experiment Video
Updated: Jun 1, 2026

Evaluation of Left Ventricular Structure and Function using 3D Echocardiography
Published on: October 28, 2020
Left ventricular noncompaction: analysis of a pediatric population
Marta António1, Carmen Costa, Margarida Venâncio
1Serviço de Cardiologia Pediátrica do Hospital Pediátrico de Coimbra, Coimbra, Portugal. marta.antonio@gmail.com
Insights
Left ventricular noncompaction (LVNC) in children often presents as congestive cardiac failure and can coexist with other cardiomyopathies. Further large-scale studies are needed to clarify diagnostic criteria for this rare condition.
Area of Science:
- Cardiology
- Pediatric Cardiology
- Genetics
Background:
- Left ventricular noncompaction (LVNC) is a rare cardiomyopathy characterized by excessive trabeculations and deep recesses.
- Diagnosis is typically aided by echocardiography and cardiac MRI, with MRI offering high sensitivity and specificity.
Purpose of the Study:
- To characterize clinical and imaging features of pediatric LVNC.
- To assess the evolution of LVNC in children.
Main Methods:
- Retrospective chart review of five pediatric patients with LVNC.
- Follow-up at Coimbra Pediatric Hospital from January 1999 to December 2007.
- Genetic analysis for MYBPC3 gene mutations.
Main Results:
- Median age at presentation was five months; most patients were male.
- Congestive cardiac failure was the most common presentation; ventricular apical involvement occurred in all cases.
- Four patients showed improved ventricular dysfunction with therapy; one case showed a phenotype change from dilated to hypertrophic, with a MYBPC3 gene mutation identified.
Conclusions:
- Congestive cardiac failure is the primary clinical presentation of pediatric LVNC, which may co-occur with dilated or hypertrophic cardiomyopathies.
- The study highlights the need for larger prospective studies to establish definitive diagnostic criteria for pediatric LVNC.
Introduction:
Left ventricular noncompaction (LVNC) is a rare and potentially progressive cardiomyopathy, characterized by the persistence of multiple trabeculations and deep intratrabecular recesses in the ventricular myocardium. Although two-dimensional and color Doppler echocardiography are the most useful diagnostic modalities, cardiac magnetic resonance imaging has proved to have high sensitivity and specificity in the diagnosis of this anomaly.
Objective:
To characterize the clinical and imaging features of LVNC in a pediatric population and to assess their evolution.
Methods And Results:
We performed a retrospective chart review of five pediatric patients with LVNC, followed at Coimbra Pediatric Hospital between January 1999 and December 2007. Median age at presentation was five months (ranging from one day to 13 years), and they were mainly male (1.5:1). Two of the children had a family history of sudden death. In one case the clinical presentation was cardiac arrest due to ventricular fibrillation and in three others, congestive cardiac failure. None of the five cases had associated congenital cardiac anomalies. Involvement of the ventricular apical region was found in all cases. Four children additionally had ventricular dysfunction which improved with diuretic and vasodilator therapy. Mean follow-up was 34 months, ranging from six months to seven years. In one case a change in the morphological phenotype was noted, from a dilated to a hypertrophic form. In this case and in the child's father a mutation in the MYBPC3 gene was identified, which is associated with hypertrophic cardiomyopathy. No thromboembolic phenomena or deaths occurred during the study period.
Conclusion:
In the pediatric population, congestive cardiac failure is the most common clinical presentation of LVNC, which can coexist with other cardiomyopathies, particularly dilated and hypertrophic forms. The sample presented in this analysis is statistically non-significant due to its limited size and the authors highlight the need for larger prospective studies in the pediatric population in order to clarify this disease and its diagnostic criteria.

