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doi: 10.1007/bf02328637
pmid: 2704655
Aortic root dilatation and mitral valve prolapse are cardiac findings sometimes seen in disorders of connective tissue, most often in the Marfan syndrome. This report describes an infant with these cardiac anomalies and a specific chromosomal abnormality, partial trisomy of chromosome 7 associated with partial monosomy of chromosome 22. This association may have significance with respect to the etiology of cardiac disease in connective tissue disorders such as Marfan syndrome.
Male, Infant, Newborn, Infant, Aorta, Thoracic, Trisomy, Marfan Syndrome, Echocardiography, Diseases in Twins, Humans, Ductus Arteriosus, Patent, Chromosomes, Human, Pair 7, Dilatation, Pathologic, Follow-Up Studies
Male, Infant, Newborn, Infant, Aorta, Thoracic, Trisomy, Marfan Syndrome, Echocardiography, Diseases in Twins, Humans, Ductus Arteriosus, Patent, Chromosomes, Human, Pair 7, Dilatation, Pathologic, Follow-Up Studies
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