作者: Ferande Peters , Bijoy K. Khandheria
DOI: 10.1007/S11886-012-0255-0
关键词:
摘要: Isolated left ventricular noncompaction (ILVNC) is a myocardial disorder thought to occur as result of an arrest in embryogenesis. Recently, it has been classified genetic cardiomyopathy. Familial and sporadic forms ILVNC have documented. There considerable heterogeneity among familial forms, although sarcomeric mutations are the most common mutations. Issues related screening require careful consideration future research. controversy regarding several aspects relating pathogenesis, diagnosis, management subjects with ILVNC. Differentiating some cases from normal variant architecture challenging requires work. This review intended provide clinicians insight into these issues offer practical guidance dealing difficult clinical scenarios.