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致心律失常性右室心肌病(纳克索斯病):一名土耳其男孩的病例报告

Arrhythmogenic right ventricular cardiomyopathy (Naxos disease): report of a Turkish boy.

作者信息

Narin Nazmi, Akcakus Mustafa, Gunes Tamer, Celiker Alpay, Baykan Ali, Uzum Kazim, Ferahbas Ayten

机构信息

Department of Pediatrics, Erciyes University, School of Medicine, Kayseri, Turkey.

出版信息

Pacing Clin Electrophysiol. 2003 Dec;26(12):2326-9. doi: 10.1111/j.1540-8159.2003.00370.x.

Abstract

Naxos disease is a recessively inherited arrhythmogenic right ventricular cardiomyopathy in which the cardiac phenotype is associated with palmoplantar keratoderma and woolly hair. This disease is a heart muscle disorder causing life-threatening ventricular arrhythmias, heart failure, and sudden cardiac death. The pathological hallmark of the disease is the progressive replacement of myocardial cells by fat and fibrous tissue. It appears in families descending from the Hellenic island of Naxos. We presented a 13-year-old Turkish boy with Naxos disease associated with ventricular tachycardia because of its rarity, and reviewed the literature.

摘要

纳克索斯病是一种隐性遗传的致心律失常性右室心肌病,其心脏表型与掌跖角化病和羊毛状发有关。这种疾病是一种心肌紊乱,可导致危及生命的室性心律失常、心力衰竭和心源性猝死。该病的病理标志是心肌细胞逐渐被脂肪和纤维组织替代。它出现在来自希腊纳克索斯岛的家族中。由于其罕见性,我们报告了一名患有与室性心动过速相关的纳克索斯病的13岁土耳其男孩,并对文献进行了回顾。

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