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Myotonic heart disease: a clinical follow-up.

作者信息

Hawley R J, Milner M R, Gottdiener J S, Cohen A

机构信息

Neurology Service, VA Medical Center, Washington, DC 20422.

出版信息

Neurology. 1991 Feb;41(2 ( Pt 1)):259-62. doi: 10.1212/wnl.41.2_part_1.259.

DOI:10.1212/wnl.41.2_part_1.259
PMID:1992371
Abstract

We followed 37 patients with myotonic dystrophy for a mean of 6 years. Two developed atrial flutter or fibrillation, 6 developed a new bundle branch block, 1 developed complete heart block requiring a pacemaker, and another with progressive 1st-degree heart block and a widening QRS interval had a sudden death. Most patients had predictable, gradually progressive disease of their cardiac conduction system. We recommend that patients with progressive atrioventricular block or widening QRS interval due to myotonic heart disease have yearly ECGs and be questioned about syncope or presyncope to determine the need for a cardiac pacemaker.

摘要

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