A Case of Hypertrophic Cardiomyopathy Associated with Wolff-Parkinson-White Syndrome
Journal of the Korean Pediatric Cardiology Society
;
: 181-186, 2004.
Artigo
em Coreano
| WPRIM
| ID: wpr-218442
ABSTRACT
Hypertrophic cardiomyopathy(HCM) is defined as a thickened wall of heart muscles and non-dilated left ventricle, but is not accompanied underlying cardiac or systemic diseases that induce ventricular hypertrophy. HCM is responsible to exercise limitation for all ages and also is known as the most common cause of heart-related sudden death during childhood and adolescents. Epidemiological studies showed that prevalence in young adults is 0.2% and HCM is caused by a mutations in genes that code the proteins of cardiac muscles. HCM with Wolff-Parkinson-White Syndrome is extremely rare and associated with a high risk of tachyarrhythmia and sudden death. We report an infantile HCM with WPW syndrome who died suddenly.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Taquicardia
/
Síndrome de Wolff-Parkinson-White
/
Cardiomiopatia Hipertrófica
/
Prevalência
/
Morte Súbita Cardíaca
/
Morte Súbita
/
Ventrículos do Coração
/
Hidrocefalia
/
Hipertrofia
/
Miocárdio
Tipo de estudo:
Estudo de prevalência
Limite:
Adolescente
/
Humanos
Idioma:
Coreano
Revista:
Journal of the Korean Pediatric Cardiology Society
Ano de publicação:
2004
Tipo de documento:
Artigo
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