Emery A E
Division of Neurology, Duke University Medical Center, Durham, North Carolina.
Clin Genet. 1987 Nov;32(5):360-7. doi: 10.1111/j.1399-0004.1987.tb03302.x.
The original Virginia family with X-linked muscular dystrophy with early contractures and cardiomyopathy (Emery-Dreifuss type) has been reinvestigated 25 years later. The findings confirm that a cardiomyopathy, presenting most often as atrioventricular block, is a significant feature of the disease, which is characterized by the triad of: 1) slowly progressive muscle wasting and weakness with a humero-peroneal distribution in the early stages; 2) early contractures of the elbows, Achilles tendons, and post-cervical muscles; and 3) a cardiomyopathy usually presenting as heart block (some female carriers may also develop heart block). Other reported families with X-linked Emery-Dreifuss muscular dystrophy as well as a rare autosomal variant are reviewed, and differentiation from scapulo-peroneal muscular dystrophy and the rigid spine syndrome is discussed.
25年后,对最初患有X连锁型肌营养不良伴早期挛缩和心肌病(埃默里-德赖富斯型)的弗吉尼亚家族进行了重新研究。研究结果证实,心肌病最常表现为房室传导阻滞,是该疾病的一个显著特征,其特点为三联征:1)早期缓慢进行性肌肉萎缩和无力,呈肱腓型分布;2)肘部、跟腱和颈后肌肉早期挛缩;3)心肌病通常表现为心脏传导阻滞(一些女性携带者也可能发生心脏传导阻滞)。本文还综述了其他报道的X连锁型埃默里-德赖富斯肌营养不良家族以及一种罕见的常染色体变异型,并讨论了与肩胛腓骨肌营养不良和僵硬脊柱综合征的鉴别。