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Mitochondrial cardiomyopathy diagnosed with histological and genetic analyses.

https://asahi-u.repo.nii.ac.jp/records/8909
https://asahi-u.repo.nii.ac.jp/records/8909
052fc784-4138-4bf7-99e1-9a9ea7e709d8
Item type 朝日大学 教育・研究業績(1)
公開日 2018-01-15
タイトル
タイトル Mitochondrial cardiomyopathy diagnosed with histological and genetic analyses.
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_1843
資源タイプ other
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
業績分類
値 学術雑誌論文
教員氏名 竹村, 元三

× 竹村, 元三

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竹村, 元三

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発行、発表雑誌等、又は発表学会等の名称
値 Case Report in Cardiology.
巻
値 2017
掲載ページ
値 9473917
単著、共著の別
値 共著
発行又は発表の年月
日付 2017
概要
値 We report a case with 46-year-old man diagnosed with mitochondrial cardiomyopathy in the dilated phase of hypertrophic cardiomyopathy. Since cardiac magnetic resonance imaging, beta-methyl-p-123I-iodophenyl-pentadecanoic myocardial scintigraphy, and positron emission tomography/computed tomography revealed no remarkable findings, we performed electron microscopic examination, which aided in diagnosing mitochondrial cardiomyopathy. Muscle biopsy was also compatible with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes and DNA analysis also concluded it. Since muscle biopsy is less invasive for patients compared to endomyocardial biopsy, cardiologists need to consider it. The diagnosis of mitochondrial cardiomyopathy is helpful because it is a genetic condition and also for consideration of device therapy, as well as management for acute crisis.
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