Abstract
An unusual type of hypertrophic cardiomyopathy was diagnosed in a 17-year-old girl who presented with dyspnea on exertion. The hypertrophied myocardium was localized to the anterior portion of the left ventricle from the base to the apex without left ventricular outflow tract obstruction. On cardiac magnetic resonance imaging (MRI), patchy and linear delayed hyperenhancement was shown in the anterior and inferior mid-wall, which is not concordant with the coronary artery territory. Copyright © 2009 The Korean Society of Cardiology.
Author supplied keywords
Cite
CITATION STYLE
Seo, H. S., Dong, H. K., Eun, J. K., Hee, Y. Y., Kim, C., Chan, H. L., … Lee, N. H. (2009). An unusual type of hypertrophic cardiomyopathy. Korean Circulation Journal, 39(5), 213–216. https://doi.org/10.4070/kcj.2009.39.5.213
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.