Author:
Shuaib Ashfaq,Martin Justin M.E.,Mitchell L. Brent,Brownell A. Keith W.
Abstract
ABSTRACT:Four patients with Multicore Myopathy, a rare morphologically distinct myopathy, are described. Although previously considered to be a non-progressive or only slowly progressive myopathy, progression to significant disability was seen in three of our cases. The association of cardiac disease with Multicore Myopathy has not been previously emphasised. All four patients in this study had a cardiomyopathy, and heart disease was the cause of death in two of the patients. Multicore Myopathy is not always a benign entity. Cardiac involvement, when present, adversely affects prognosis.
Publisher
Cambridge University Press (CUP)
Subject
Clinical Neurology,Neurology,General Medicine
Reference27 articles.
1. The Pathogenesis of Cardiac Cachexia
2. Congenital myopathy associated with focal degeneration of muscle fibres;Engel;Trans Am Neurol Assn,1966
3. Scapuloperoneal Muscular Atrophy With Cardiopathy
Cited by
31 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献