Gallai V, Rossi A, Cianchetti A, Morocutti C, Vaccario M L
Riv Patol Nerv Ment. 1977 Nov-Dec;98(6):333-46.
Clinical, electromyographic, histochemical and ultrastructural features are described in a case of Chronic Progressive Ophthalmoplegia. The neurogenic-myogenic aspects of the diseases are discussed bearing in mind both electromyographic and histological findings ("red ragged fibres" etc.). Mitochondrial paracrystalline inclusions were found at the level of the ocular muscles as well as in the skeletal muscles. These inclusione suggest that Ocular Myopathy is a form of systemic myopathy secondary to mitochondrial abnormalities.
本文描述了一例慢性进行性眼肌麻痹患者的临床、肌电图、组织化学和超微结构特征。结合肌电图和组织学检查结果（“红色破碎纤维”等），对该疾病的神经源性-肌源性方面进行了讨论。在眼肌和骨骼肌中均发现了线粒体副结晶包涵体。这些包涵体提示眼肌病是继发于线粒体异常的一种全身性肌病。
