原发性致心律失常性左心室心肌病伴心脏皮肤表型——卡瓦哈尔综合征的心脏磁共振成像表现 - Suppr

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超能文献

Cardiac magnetic resonance imaging findings in primary arrhythmogenic left ventricular cardiomyopathy with cardiocutaneous phenotype-Carvajal syndrome.

作者信息

Akintoye Emmanuel, Ashwath Mahi L

机构信息

Division of Cardiovascular Medicine, University of Iowa Hospitals and Clinics, Iowa City, Iowa.

出版信息

HeartRhythm Case Rep. 2021 Feb 10;7(5):312-315. doi: 10.1016/j.hrcr.2021.01.024. eCollection 2021 May.

DOI:10.1016/j.hrcr.2021.01.024

PMID:34026522

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8134784/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d225/8134784/a0f2ade68a3e/gr1.jpg

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本文引用的文献

Diagnosis of arrhythmogenic cardiomyopathy: The Padua criteria.心律失常性心肌病的诊断：帕多瓦标准。

Int J Cardiol. 2020 Nov 15;319:106-114. doi: 10.1016/j.ijcard.2020.06.005. Epub 2020 Jun 16.

Dilated cardiomyopathy and arrhythmogenic left ventricular cardiomyopathy: a comprehensive genotype-imaging phenotype study.扩张型心肌病和致心律失常性左室心肌病：一项综合的基因型-影像表型研究。

Eur Heart J Cardiovasc Imaging. 2020 Mar 1;21(3):326-336. doi: 10.1093/ehjci/jez188.

2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy.2019 HRS 专家共识声明：心律失常性心肌病的评估、风险分层和管理。

Heart Rhythm. 2019 Nov;16(11):e301-e372. doi: 10.1016/j.hrthm.2019.05.007. Epub 2019 May 9.

A novel genotype-based clinicopathology classification of arrhythmogenic cardiomyopathy provides novel insights into disease progression.一种基于新型基因型的心律失常性心肌病临床病理分类为疾病进展提供了新的见解。

Eur Heart J. 2019 Jun 1;40(21):1690-1703. doi: 10.1093/eurheartj/ehz172.

Images in cardiovascular medicine. Magnetic resonance imaging characteristics in Carvajal syndrome (variant of Naxos disease).

Circulation. 2007 Nov 13;116(20):e524-30. doi: 10.1161/CIRCULATIONAHA.107.704742.

Novel mutation in desmoplakin causes arrhythmogenic left ventricular cardiomyopathy.桥粒斑蛋白的新型突变导致致心律失常性左室心肌病。

Circulation. 2005 Aug 2;112(5):636-42. doi: 10.1161/CIRCULATIONAHA.104.532234.

Cardiovasc Pathol. 2004 Jul-Aug;13(4):185-94. doi: 10.1016/j.carpath.2004.03.609.

A recessive mutation in desmoplakin causes arrhythmogenic right ventricular dysplasia, skin disorder, and woolly hair.桥粒斑蛋白中的隐性突变会导致致心律失常性右心室发育不良、皮肤疾病和羊毛状毛发。

J Am Coll Cardiol. 2003 Jul 16;42(2):319-27. doi: 10.1016/s0735-1097(03)00628-4.

Epidermolytic palmoplantar keratoderma with woolly hair and dilated cardiomyopathy.伴有羊毛状毛发和扩张型心肌病的表皮松解性掌跖角化病。

J Am Acad Dermatol. 1998 Sep;39(3):418-21. doi: 10.1016/s0190-9622(98)70317-2.

Familial occurrence of a rare combination of dilated cardiomyopathy with palmoplantar keratoderma and curly hair.扩张型心肌病合并掌跖角化病和卷发的罕见组合的家族性发病情况。

Indian Heart J. 1996 Mar-Apr;48(2):161-2.

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