Korean J Perinatol.  2003 Dec;14(4):447-451.

Prenatal Diagnosis in a Case of Familial Hypertrophic Cardiomyopathy by Prenatal Ultrasonography

Affiliations
  • 1Department of Obstetrics and Gynecology, College of Medicine, University of Ulsan, Asan Medical Center, Seoul, Korea. hswon@amc.seoul.kr

Abstract

About half of all cases of hypertrophic cardiomyopathy(HCMP) have a positive family history. All first-degree relatives of patients with HCMP should be screened with echocardiography. The prenatal diagnosis of abnormal septal hypertrophy in fetuses of mothers with HCMP has not yet been documented. We report a prenatal diagnosis in a case of familial HCMP by ultrasonography which was confirmed by autopsy. Fetal echocardiography provides a valuable aid in diagnosis of familial HCMP.

Keyword

Familial hypertrophic cardiomyopathy; Prenatal ultrasonography

MeSH Terms

Autopsy
Cardiomyopathy, Hypertrophic, Familial*
Diagnosis
Echocardiography
Fetus
Humans
Hypertrophy
Mothers
Prenatal Diagnosis*
Ultrasonography
Ultrasonography, Prenatal*
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