A rare case: Coexistence of noncompaction cardiomyopathy and Ebstein anomaly

Noncompaction cardiomyopathy is a rare type of that can result in left ventricular failure, thromboembolic events, tachyarrhythmias, and sudden cardiac death. It congenital which deep trabeculations cavities the ventricle are formed due to cessation development myocardial tissue intrauterine period. Ebstein's anomaly characterized by apical displacement tricuspid valve septal leaflet. Although association noncompaction ebstein disease, there cases described literature. A 23-year-old male patient, who presented with palpitations fatigue, was diagnosed anomaly. After diagnosis, patient followed closely without complications appropriate medical follow-up. Congenital heart diseases be seen alone or other malformations. When suspicious findings ebstein's anomaly, it may associated cardiomyopathy, screening echocardiographic MRI should considered.