Witt T N, Garner C G, Pongratz D, Baur X
Neurologische Klinik, Klinikum Grosshadern, München, Federal Republic of Germany.
Eur Arch Psychiatry Neurol Sci. 1988;237(4):230-6. doi: 10.1007/BF00449912.
The first German family with autosomal dominant Emery-Dreifuss syndrome (EDS) is described, with electrophysiologic and myopathologic results providing evidence of a primary neurogenic disease. According to classification of the scapulo peroneal syndrome without cardiomyopathy, we conclude that there are two variants of EDS: one myopathic, the other neurogenic in origin. Therefore, the term Emery-Dreifuss muscular dystrophy should be avoided. Instead, each case of EDS should be classified as myopathic or neurogenic with X chromosome recessive or autosomal dominant inheritance.
本文描述了首个患常染色体显性遗传埃默里-德赖富斯综合征(EDS)的德国家庭,其电生理和肌病学结果为原发性神经源性疾病提供了证据。根据无心肌病的肩胛腓骨综合征的分类,我们得出结论,EDS有两种变体:一种源于肌病,另一种源于神经源性。因此,应避免使用埃默里-德赖富斯肌营养不良症这一术语。相反,每例EDS应根据X染色体隐性或常染色体显性遗传分为肌病性或神经源性。