Familial left ventricular noncompaction associated with a novel mutation in the alpha-cardiac actin gene.
نویسندگان
چکیده
4. Gold MR, Birgersdotter-Green U, Singh JP, Ellenbogen KA, Yu Y, Meyer TE, et al. The relationship between ventricular electrical delay and left ventricular remodelling with cardiac resynchronization therapy. Eur Heart J. 2011;32:2516–24. 5. Kristiansen HM, Hovstad T, Vollan G, Keilegavlen H, Faerestrand S. Clinical 6. Miranda RI, Nault M, Johri A, Simpson CS, Michael KA, Abdollah H, et al. Maxim electric separation-guided placement of right ventricular lead improves re sponders in cardiac resynchronization defibrillator therapy. Circ Arrhythm Electrophysiol. 2012;5:927–32.
منابع مشابه
Novel α‐Actin Gene Mutation p.(Ala21Val) Causing Familial Hypertrophic Cardiomyopathy, Myocardial Noncompaction, and Transmural Crypts. Clinical‐Pathologic Correlation
BACKGROUND Mutations of α-actin gene (ACTC1) have been phenotypically related to various cardiac anomalies, including hypertrophic cardiomyopathy and dilated cardiomyopathy and left ventricular (LV) myocardial noncompaction. A novel ACTC mutation is reported as cosegregating for familial hypertrophic cardiomyopathy and LV myocardial noncompaction with transmural crypts. METHODS AND RESULTS In...
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عنوان ژورنال:
- Revista espanola de cardiologia
دوره 67 10 شماره
صفحات -
تاریخ انتشار 2014