Diverse manifestation of arrhythmogenic right ventricular dysplasia in a family.
J Indian Med Assoc
;
2000 Nov; 98(11): 730-2, 735
Artículo
en Inglés
| IMSEAR
| ID: sea-104453
ABSTRACT
Arrhythmogenic right ventricular dysplasia (ARVD) is a cardiomyopathy of unknown cause associated with life-threatening arrhythmias. The purpose of this case report is two-fold (i) To highlight the utility of a definite set of diagnostic criteria encompassing structural, histologic, electrocardiographic, arrhythmic and genetic factors in establishing diagnosis of ARVD in institutions like ours which are handicapped by lack of magnetic resonance imaging (MRI) and endomyocardial biopsy facilities, (ii) to present diverse arrhythmic manifestations in a single family.
Texto completo:
Disponible
Índice:
IMSEAR (Asia Sudoriental)
Asunto principal:
Humanos
/
Masculino
/
Ecocardiografía Doppler
/
Núcleo Familiar
/
Adolescente
/
Displasia Ventricular Derecha Arritmogénica
/
Electrocardiografía
Idioma:
Inglés
Revista:
J Indian Med Assoc
Año:
2000
Tipo del documento:
Artículo
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