Infantile hypertrophic cardiomyopathy with QT prolongation.
スポンサーリンク
概要
- 論文の詳細を見る
An infant who died at 5 months with hypertrophic cardiomyopathy accompanied by QT prolongation was examined at autopsy. At the age of 16 days, serum IgM level was elevated (226mg/dl). Microscopic examination revealed characteristics of hypertrophic cardiomyopathy with myocardial cell hypertrophy with disarray and healed myocarditis with patchy fibrosis and mononuclear cell infiltration. The histological findings were compatible with those of postmyocarditic cardiomegaly developing during the fetal period.
- International Heart Journal刊行会の論文
著者
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Yabuta Keijiro
Department Of Pediatrics Juntendo University Of School Medicine
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Ino Toshihiro
Department of Pediatrics, Juntendo University School of Medicine
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EGUCHI Masanobu
Department of Pathology, Juntendo University School of Medicine
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Nishimoto Kei
Department Of Pediatrics Juntendo University School Of Medicine
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Eguchi Masanobu
Department Of Pathology Juntendo Izu-nagaoka Hospital Juntendo University School Of Medicine
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Akimoto Katsumi
Department Of Pediatrics Juntendo University School Of Medicine
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Iwahara Masazumi
Department Of Pediatrics Juntendo University
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Okada Ryozo
Department Of Cardiology Juntendo University School Of Medicine
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INO Toshihiro
Department of Pediatrics and the Juntendo University School of Medicine
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YABUTA Keijiro
Department of Pediatrics and the Juntendo University School of Medicine
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