Noncompaction of the Ventricular Myocardium and Polycystic Kidney Disease: A Case Report
作者： Keiko Fukino , Junpei Ishiwata , Hiroki Shinohara , Tsukasa Oshima , Tsunashi Kozaki
DOI: 10.1053/J.AJKD.2015.12.031
关键词: Aneurysm 、 Internal medicine 、 Autosomal dominant polycystic kidney disease 、 Medicine 、 Polycystic kidney disease 、 Aortic aneurysm 、 Cardiomyopathy 、 Cardiology 、 Ventricular aneurysm 、 Disease 、 Left Ventricular Aneurysm
摘要: Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common hereditary disorders, characterized by formation multiple cysts in kidneys and other organs, as well noncystic manifestations such cerebral aneurysm. The cardiovascular disorders associated with ADPKD include valvular abnormalities aortic An association between impaired left ventricular function has occasionally been reported. We describe a 74-year-old woman exertional dyspnea. Impaired resulting from noncompaction myocardium (NVM) secondary aneurysm were diagnosed. Cardiac sarcoidosis ischemic heart ruled out. Myocardial ischemia NVM was presumptive cause To our knowledge, this first report concurrent isolated patient ADPKD. various cardiomyopathies, including NVM, are all reported to involve mutations sarcomere genes, suggesting possible link conditions.
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