Myocardial involvement in the Marfan syndrome.
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概要
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A patient with the Marfan syndrome and echocardiographic and angiocardiographic evidence of hypertrophic cardiomyopathy is presented. Endomyocardial biopsy was performed. Histologic abnormalities of the endomyocardium noted in this patient were considered to be related to the basic generalized connective tissue abnormality, and the patient subsequently developed myocardial disease compatible with hypertrophic non-obstructive cardiomyopathy. We believe that this case emphasizes the possible coexistance of subclinical myocardial disease in patients with the Marfan syndrome.
- International Heart Journal刊行会の論文
著者
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Kawanishi Katsuyuki
Department Of Radiology Shiga University Of Medical Science
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Okuno Keiko
Department Of Internal Medicine National Hospital Organization Kobe Medical Center
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Shimada Morimi
Department Of Pediatrics Shiga Medical College
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Fujiseki Yoshiki
Department of Pediatrics Shiga University of Medical Science
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Tanaka Masaki
Department Of Anatomy & Neurobiology Kyoto Prefectural University Of Medicine
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Takahashi Masashi
Department Of Animal And Grassland Research National Agricultural Center For Kyushu Okinawa Region
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FUJISEKI Yoshiki
Department of Pediatrics, Shiga University of Medical Science
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OKUNO Keiko
Department of Pediatrics, Shiga University of Medical Science
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