可逆性心肌病,临床医生应注意什么?一个病例报告。

IF 0.7 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS Journal of the Saudi Heart Association Pub Date : 2023-01-01 DOI:10.37616/2212-5043.1339
Abdulmajeed A Alzahrani, Saud A Bahaidarah, Zuhair N Al-Hassnan, Gaser A Abdelmohsen
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引用次数: 0

摘要

原发性肉碱缺乏症(PCD)是一种常染色体隐性遗传病,其特征是包括心脏在内的各器官中β氧化所必需的肉碱水平降低。PCD的早期诊断和治疗可使心肌病恢复。一例13岁女孩因扩张性心肌病和严重心功能障碍导致心力衰竭;经左旋肉碱治疗后,患者临床情况改善,心功能在数周内恢复正常。调查发现PCD;已提供常规左旋肉碱,所有心脏药物已停用,病人情况良好。我们认为所有心肌病患者都应排除PCD。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Reversible Cardiomyopathy, What Should the Clinicians Keep in Mind? A Case Report.

Primary carnitine deficiency (PCD) is an autosomal recessive disorder characterized by decreased carnitine levels essential for Beta oxidation in various organs, including the heart. Early diagnosis and treatment of PCD can revert cardiomyopathy. A 13-year-old girl presented with heart failure due to dilated cardiomyopathy and severe cardiac dysfunction; following L carnitine treatment, the patient's clinical conditions improved, and cardiac functions returned to normal within weeks. Investigations revealed PCD; regular L carnitine has been provided, all cardiac medications are discontinued, and the patient is doing well. We believe PCD should be ruled out in every patient with cardiomyopathy.

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来源期刊
Journal of the Saudi Heart Association
Journal of the Saudi Heart Association CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
1.40
自引率
0.00%
发文量
30
审稿时长
15 weeks
期刊最新文献
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