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.
|Number of pages||3|
|Journal||Korean Circulation Journal|
|Publication status||Published - 2013 Jan|
- Cardiomyopathy, hypertrophic
ASJC Scopus subject areas
- Internal Medicine
- Cardiology and Cardiovascular Medicine