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Arq. bras. cardiol ; 75(4): 323-8, Oct. 2000.
Article in Portuguese, English | LILACS | ID: lil-272692

ABSTRACT

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


Subject(s)
Humans , Male , Adult , Abnormalities, Multiple/diagnosis , Heart Defects, Congenital/diagnosis , Syndrome
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