Sudden cardiac death in neuromuscular disorders

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Sudden cardiac death in neuromuscular disorders

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作者：Josef Finsterer^a ; ^{fifigs1@yahoo.de" class="auth_mail" title="E-mail the corresponding author} ; Claudia Stö ; llberger^b ; Concha Maeztu^c
关键词：ALS ; amyotrophic lateral sclerosis ; ARVC ; arrhythmogenic right ventricular cardiomyopathy ; ATS ; Andersen&ndash ; Tawil syndrome ; BBB ; bundle branch block ; BMD ; Becker muscular dystrophy ; CACT ; carnitine-acylcarnitine translocase ; cMRI ; cardiac magnetic resonance imaging ; CNS ; central nervous system ; dCMP ; dilated cardiomyopathy ; DM1 ; myotonic dystrophy type 1 ; DM2 ; myotonic dystrophy type 2 ; DMD ; Duchenne muscular dystrophy ; ECG ; Electrocardiography ; EF ; Ejection fraction ; FAP ; Familial amyloid po
刊名：International Journal of Cardiology
出版年：2016
出版时间：15 January 2016
年：2016
卷：203
期：Complete
页码：508-515
全文大小：517 K

文摘

•: Patients with certain neuromuscular disorders carry an increased risk to experience sudden cardiac death
•: Risk of SCD is particularly increased in myotonic dystrophy, mitochondrial disorders, laminopathies, and desminopathies.
•: Risk factors to develop sudden cardiac death vary considerably between neuromuscular disorders.
•: Risk factors for SCD include fibrosis, QT-prolongation, increased QT-dispersion, early repolarization, or T-wave alternans.

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