A case of congenital hypertrophic cardiomyopathy

Hyeon Seok Seo; In Hak Lee; Young Wooh Song; Byung Min Choi; Gi Young Jang; Chang Sung Son; Joo Won Lee

doi:10.4070/kcj.2013.43.1.54

A case of congenital hypertrophic cardiomyopathy

Hyeon Seok Seo, In Hak Lee, Young Wooh Song, Byung Min Choi, Gi Young Jang, Chang Sung Son, Joo Won Lee

Research output: Contribution to journal › Article › peer-review

1 Citation (Scopus)

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.

Original language	English
Pages (from-to)	54-56
Number of pages	3
Journal	Korean Circulation Journal
Volume	43
Issue number	1
DOIs	https://doi.org/10.4070/kcj.2013.43.1.54
Publication status	Published - 2013 Jan

Keywords

Cardiomyopathy, hypertrophic
Newborns

ASJC Scopus subject areas

Internal Medicine
Cardiology and Cardiovascular Medicine

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10.4070/kcj.2013.43.1.54

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title = "A case of congenital hypertrophic cardiomyopathy",

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.",

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AU - Seo, Hyeon Seok

AU - Lee, In Hak

AU - Song, Young Wooh

AU - Choi, Byung Min

AU - Jang, Gi Young

AU - Son, Chang Sung

AU - Lee, Joo Won

PY - 2013/1

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N2 - 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.

AB - 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.

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KW - Newborns

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A case of congenital hypertrophic cardiomyopathy

Abstract

Keywords

ASJC Scopus subject areas

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