Article
Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7.
American journal of medical genetics. Part C, Seminars in medical genetics - 1 Aug 2013
Vermeer Alexa M C, van Engelen Klaartje, Postma Alex V, Baars Marieke J H, Christiaans Imke, De Haij Simone, Klaassen Sabine, Mulder Barbara J M, Keavney Bernard
Abstract excerpt
Left ventricular noncompaction (LVNC) is a relatively common genetic cardiomyopathy, characterized by prominent trabeculations with deep intertrabecular recesses in mainly the left ventricle. Although LVNC often occurs in an isolated entity, it may also be present in various types of congenital heart disease (CHD). The most prevalent CHD in LVNC is Ebstein anomaly, which is a rare form of CHD characterized by...
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