Argov Z, Yarom R
J Neurol Sci. 1984 Apr;64(1):33-43. doi: 10.1016/0022-510x(84)90053-4.
Nine cases from 4 different Iranian-Jewish families presented with generalized muscular weakness. Quadriceps muscle was the only leg muscle which retained its normal power and function even in advanced cases. Biopsies from severely involved muscles revealed a typical "rimmed vacuole myopathy" while the quadriceps and deltoid showed minimal changes. CK levels were normal or moderately elevated and the EMG pattern suggested an underlining neurogenic disorder. The possible neurogenic character of this autosomal recessive disorder is discussed with relevance to the rimmed vacuoles.
来自4个不同伊朗犹太家庭的9例患者表现为全身肌肉无力。即使在病情晚期,股四头肌仍是唯一保持正常力量和功能的腿部肌肉。严重受累肌肉的活检显示典型的“镶边空泡肌病”,而股四头肌和三角肌变化最小。肌酸激酶水平正常或中度升高,肌电图模式提示潜在的神经源性疾病。本文结合镶边空泡探讨了这种常染色体隐性疾病可能的神经源性特征。