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Autor:
Sandro Mario Belforte, Tomás F. Cianciulli, Victorio Próspero Picone, Eduardo Fernandez Rostello, Horacio A. Prezioso, Jorge A. Lax, Héctor Jorge Redruello, Barbara Recalde
Publikováno v:
European Journal of Echocardiography. 8:302-306
Marfan's syndrome is a hereditary connective tissue disease, in which cardiovascular abnormalities (especially aortic root dilatation) are the most important cause of morbidity and mortality. In this report, we describe two 24-year-old twins, with a