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A Case of Congenital Hypertrophic Cardiomyopathy
Article in English | WPRIM (Western Pacific) | ID: wpr-214108
Responsible library: WPRO
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.
Subject(s)

Full text: Available Database: WPRIM (Western Pacific) Main subject: Autopsy / Cardiomyopathy, Hypertrophic / Echocardiography / Heart Diseases / Heart Failure Limits: Humans / Infant, Newborn Language: English Journal: Korean Circulation Journal Year: 2013 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Main subject: Autopsy / Cardiomyopathy, Hypertrophic / Echocardiography / Heart Diseases / Heart Failure Limits: Humans / Infant, Newborn Language: English Journal: Korean Circulation Journal Year: 2013 Document type: Article
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