Left ventricular noncompaction in a family with lamin A/C gene mutation.


Left ventricular noncompaction is a rare type of cardiomyopathy, the genetics of which are poorly understood to date. Lamin A/C gene mutations have been associated with dilated cardiomyopathy and diseases of the conduction system, but rarely in left ventricular noncompaction cardiomyopathy. This report describes the cases of 4 family members with a lamin A… (More)
DOI: 10.14503/THIJ-13-3843


4 Figures and Tables