Heritable Q-T Prolongation without Deafness : The Romano-Ward Syndrome
スポンサーリンク
概要
- 論文の詳細を見る
This paper deals with 2 female cases, aged 21 and 17, diagnosed as the Romano-Ward syndrome. They belonged to different families. Both showed autosomal dominant inheritant traits. From their traits one case (Case 1) was suspected as being in the heterozygous state, while the other (Case 2) in the homozygous. The severity in clinical symptoms did not differ from each other. By studying our cases and the literature so far published, the combined use of propranolol, diphenylhydantoin, and phenobarbital was inferred to act effectively for the prevention of arrhythmias seen in the present syndrome.
- International Heart Journal刊行会の論文
著者
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Takeuchi Ayako
Department Of Pharmacy Kyoto University Hospital
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HANAZONO Naoto
The 1st Dept. Intern. Med. Tottori Univ. School of Med
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Ando Yoshihiro
Department Of Pediatrics Aichi Children's Health And Medical Center
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NISHIO Takashi
Department of Applied Physics, Faculty of Science, Fukuoka University
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HANAZONO Naoto
Department of Internal Medicine, Tottori University School of Medicine
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ODA Hiromu
Department of Internal Medicine, Tottori University School of Medicine
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ISHIDA Hisaichi
Department of Internal Medicine, Tottori University School of Medicine
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OHNISHI Mihoe
Department of Internal Medicine, Tottori University School of Medicine
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YUHARA Noriji
Department of Internal Medicine, Tottori University School of Medicine
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KOHASHI Kazunari
Department of Internal Medicine, Tottori University School of Medicine
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TAKEUCHI Ayako
Department of Internal Medicine, Tottori University School of Medicine
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NISHIO Takashi
Department of Internal Medicine, Tottori University School of Medicine
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ANDO Yoshihiro
Department of Internal Medicine, Tottori University School of Medicine
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