Abstract
Congenital hypertrophic cardiomyopathy (HCMP) is a very rare congenital heart disease. Here, we report a case of neonatal HCMP, which was confirmed by two-dimensional echocardiography and autopsy. The HCMP rapidly progressed and the patient's condition deteriorated, despite the treatment for congestive heart failure. Copyright © 2013 The Korean Society of Cardiology.
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APA
Seo, H. S., Lee, I. H., Song, Y. W., Choi, B. M., Jang, G. Y., Son, C. S., & Lee, J. W. (2013). A case of congenital hypertrophic cardiomyopathy. Korean Circulation Journal, 43(1), 54–56. https://doi.org/10.4070/kcj.2013.43.1.54
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