作者: A. Kalayci , Y. Guler , C.Y. Karabay , A. Guler , S.M. Aung
DOI: 10.1007/S00059-012-3667-0
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摘要: Noncompaction cardiomyopathy, a rare congenital is characterized by increased trabeculation in one or more segments of the ventricle. The coexistence other cardiac anomalies such as coronary-cameral fistula, bicuspid aortic valve, ventricular septal defect, patent ductus arteriosus and bradyarrhythmias make noncompaction cardiomyopathy resemble reptile heart. defect myocardial compaction frequently seen accompanying may share common causative factor during embryogenesis.