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1.
Clin Cardiol ; 19(5): 429-32, 1996 May.
Article in English | MEDLINE | ID: mdl-8723605

ABSTRACT

An unusual case of cyanosis and patent foramen ovale/atrial septal defect with right-sided septal hypertrophy is presented. Mild right ventricular dysfunction led to predominant right-to-left shunting. The atrial defect was surgically closed. The patient is from a family with hypertrophic cardiomyopathy; she is negative for the gene abnormality.


Subject(s)
Heart Defects, Congenital/etiology , Heart Septal Defects, Atrial/complications , Hypertrophy, Right Ventricular/complications , Adult , Echocardiography, Transesophageal , Electrocardiography , Female , Heart Defects, Congenital/diagnostic imaging , Heart Defects, Congenital/physiopathology , Heart Septal Defects, Atrial/diagnostic imaging , Heart Septal Defects, Atrial/physiopathology , Humans , Hypertrophy, Right Ventricular/diagnostic imaging , Hypertrophy, Right Ventricular/physiopathology , Oxygen/blood
4.
Chest ; 72(6): 774-6, 1977 Dec.
Article in English | MEDLINE | ID: mdl-923312

ABSTRACT

Coronary arterial dissection is extremely rare. Such dissections have been reported to occur secondary to atherosclerosis, trauma, the postpartum state, and cystic medial necrosis and to be iatrogenically induced during catheterization. The clinical picture of coronary arterial dissection is usually sudded death. A review of the literature reveals that our case is the second in which a spontaneous coronary arterial dissection has been diagnosed during life and documented by coronary arteriographic studies. This report describes a 31-year-old man who presented with an acute inferior myocardial infarction. Coronary arteriographic studies demonstrated a dissection of the right coronary artery.


Subject(s)
Aortic Dissection/diagnostic imaging , Coronary Angiography , Adult , Aortic Dissection/complications , Coronary Disease/complications , Coronary Disease/diagnostic imaging , Humans , Male , Myocardial Infarction/etiology
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