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Late-onset Fabry disease revealed by ventricular tachycardia: A case report.

作者信息

Ditac Geoffroy, Gardey Kévin, Jobbé-Duval Antoine, Fouilhoux Alain, Millat Gilles, Chevalier Philippe

机构信息

Service de Rythmologie, Hôpital Cardiologique Louis Pradel, Hospices Civils de Lyon, Lyon, France.

Service d'Insuffisance Cardiaque, Hôpital Cardiologique Louis Pradel, Hospices Civils de Lyon, Lyon, France.

出版信息

HeartRhythm Case Rep. 2021 Dec 3;8(2):79-83. doi: 10.1016/j.hrcr.2021.11.025. eCollection 2022 Feb.

DOI:10.1016/j.hrcr.2021.11.025
PMID:35242543
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8858774/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e014/8858774/4db91819f8c1/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e014/8858774/04a12d107670/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e014/8858774/ea833f44b374/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e014/8858774/4db91819f8c1/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e014/8858774/04a12d107670/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e014/8858774/ea833f44b374/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e014/8858774/4db91819f8c1/gr3.jpg

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本文引用的文献

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Molecular Diagnosis of Inherited Cardiac Diseases in the Era of Next-Generation Sequencing: A Single Center's Experience Over 5 Years.遗传性心脏病的分子诊断:5 年单中心经验。
Mol Diagn Ther. 2021 May;25(3):373-385. doi: 10.1007/s40291-021-00530-w. Epub 2021 May 5.
2
Radiofrequency ablation of ventricular tachycardia in Anderson-Fabry disease: a case series.安德森-法布里病中心室性心动过速的射频消融:病例系列
Eur Heart J Case Rep. 2021 Feb 4;5(2):ytaa529. doi: 10.1093/ehjcr/ytaa529. eCollection 2021 Feb.
3
Fabry disease in cardiology practice: Literature review and expert point of view.
《心脏病学实践中的法布里病:文献综述和专家观点》。
Arch Cardiovasc Dis. 2019 Apr;112(4):278-287. doi: 10.1016/j.acvd.2019.01.002. Epub 2019 Feb 28.
4
Ventricular arrhythmia and sudden cardiac death in Fabry disease: a systematic review of risk factors in clinical practice.法布瑞病患者的室性心律失常和心源性猝死:临床实践中风险因素的系统综述。
Europace. 2018 Sep 1;20(FI2):f153-f161. doi: 10.1093/europace/eux261.
5
The validation of pharmacogenetics for the identification of Fabry patients to be treated with migalastat.用于识别拟接受米加司他治疗的法布里病患者的药物遗传学验证。
Genet Med. 2017 Apr;19(4):430-438. doi: 10.1038/gim.2016.122. Epub 2016 Sep 22.
6
Genetic Screening of Anderson-Fabry Disease in Probands Referred From Multispecialty Clinics.从多专科诊所转介的先证者中进行安德森-法布里病的基因筛查。
J Am Coll Cardiol. 2016 Sep 6;68(10):1037-50. doi: 10.1016/j.jacc.2016.05.090.
7
Arrhythmias in Fabry cardiomyopathy.法布里心肌病中的心律失常
Card Electrophysiol Clin. 2015 Jun;7(2):283-91. doi: 10.1016/j.ccep.2015.03.014. Epub 2015 Apr 1.
8
2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC).2014年欧洲心脏病学会(ESC)肥厚型心肌病诊断和治疗指南:欧洲心脏病学会(ESC)肥厚型心肌病诊断和治疗工作组
Eur Heart J. 2014 Oct 14;35(39):2733-79. doi: 10.1093/eurheartj/ehu284. Epub 2014 Aug 29.
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Functional characterisation of alpha-galactosidase a mutations as a basis for a new classification system in fabry disease.以α-半乳糖苷酶 A 突变的功能特征为基础的法布里病新分类系统。
PLoS Genet. 2013;9(8):e1003632. doi: 10.1371/journal.pgen.1003632. Epub 2013 Aug 1.
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