{"title":"孤立形式的左心室非压实性心肌病(LVNC)是一种罕见的心力衰竭原因","authors":"Skopoulis Sotiris","doi":"10.5772/INTECHOPEN.76379","DOIUrl":null,"url":null,"abstract":"Non-compaction cardiomyopathy (LVNC) is a rare, hereditary disease manifested by heart failure, thromboembolic complications and arrhythmias, which can even result in a sudden cardiac arrest. This disease is often misdiagnosed as dilated or ischemic cardiomyopathy, apical hypertrophic cardiomyopathy, or other myocardial infiltrative processes, including tumours. Due to its potentially severe complications and outcomes it should be always considered as a part of differential diagnosis.","PeriodicalId":213648,"journal":{"name":"Current Perspectives on Cardiomyopathies","volume":"77 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Isolated Form of Left Ventricular Non-compaction Cardiomyopathy (LVNC) as a Rare Cause of Heart Failure\",\"authors\":\"Skopoulis Sotiris\",\"doi\":\"10.5772/INTECHOPEN.76379\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Non-compaction cardiomyopathy (LVNC) is a rare, hereditary disease manifested by heart failure, thromboembolic complications and arrhythmias, which can even result in a sudden cardiac arrest. This disease is often misdiagnosed as dilated or ischemic cardiomyopathy, apical hypertrophic cardiomyopathy, or other myocardial infiltrative processes, including tumours. Due to its potentially severe complications and outcomes it should be always considered as a part of differential diagnosis.\",\"PeriodicalId\":213648,\"journal\":{\"name\":\"Current Perspectives on Cardiomyopathies\",\"volume\":\"77 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-09-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Perspectives on Cardiomyopathies\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5772/INTECHOPEN.76379\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Perspectives on Cardiomyopathies","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5772/INTECHOPEN.76379","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Isolated Form of Left Ventricular Non-compaction Cardiomyopathy (LVNC) as a Rare Cause of Heart Failure
Non-compaction cardiomyopathy (LVNC) is a rare, hereditary disease manifested by heart failure, thromboembolic complications and arrhythmias, which can even result in a sudden cardiac arrest. This disease is often misdiagnosed as dilated or ischemic cardiomyopathy, apical hypertrophic cardiomyopathy, or other myocardial infiltrative processes, including tumours. Due to its potentially severe complications and outcomes it should be always considered as a part of differential diagnosis.