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Arq. bras. cardiol ; 75(4): 323-8, Oct. 2000.
Artículo en Portugués, Inglés | LILACS | ID: lil-272692

RESUMEN

Cantrell syndrome is characterized by defects that involve the diaphragm, abdominal wall, pericardium, heart, and lower region of the sternum. It is a rare entity, usually diagnosed at birth and accompanied by high mortality due to the complexity and gravity of the anomalies. In this report, we present a 32-year-old male patient, who was diagnosed in infancy but who reached adult age asymptomatic


Asunto(s)
Humanos , Masculino , Adulto , Anomalías Múltiples/diagnóstico , Cardiopatías Congénitas/diagnóstico , Síndrome
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