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

Abstract excerpt

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/C gene mutation, 3 of whom had phenotypic expression of...

Topics

Share this publication in a Topic to start or enrich a Post.

• Share to Adolescent
• Share to Child
• Share to DNA Mutational Analysis