Delwaide P J, Reznik M
Acta Neurol Belg. 1976 Jul-Aug;76(4):212-9.
The authors report the clinical history of a young athlete who, without any notable family antecedents, developed cardiomyopathy followed by proximal anyotrophy at the age of 24 years. The electromyogram revealed frequent myotonic salves and a typically myogenic tracing. The autopsy showed substantial generalized cardiac enlargement and marked atrophy of the muscle fibres in the girdles, together with grouping of the nuclei into hyperchromatic clusters. The reported case thus shows some characteristics of Steinet's disease and others of non-dystrophic myotonia (Becker, 1964) but cannot be classified as either of these diseases.
作者报告了一名年轻运动员的临床病史，该运动员没有任何明显的家族病史，在24岁时患上心肌病，随后出现近端肌萎缩。肌电图显示频繁的肌强直波和典型的肌源性描记。尸检显示心脏普遍显著增大，肩胛带肌纤维明显萎缩，细胞核聚集成深染簇。因此，报告的病例显示出施泰纳特病的一些特征以及非营养不良性肌强直（贝克尔，1964年）的其他特征，但不能归类为这两种疾病中的任何一种。
