Gabriel M, Lenard H G, Goebel H H
Klin Padiatr. 1978 Sep;190(5):441-5.
The case of a 16-year-old boy with progressive external ophthalmoplegia ("Ophthalmoplegia plus") is reported. Clinical symptoms consisted of complete external ophthalmoplegia, ptosis, short stature, atrophy and weakness of skeletal muscles, and elevated csf protein. Abnormal mitochondria were found by electron microscopy in scattered atrophic fibres of the muscle biopsy. The syndrome and it's relevance for paediatric differential diagnosis is discussed.
报告了一名16岁患有进行性眼外肌麻痹(“眼肌麻痹加综合征”)男孩的病例。临床症状包括完全性眼外肌麻痹、上睑下垂、身材矮小、骨骼肌萎缩和无力以及脑脊液蛋白升高。通过电子显微镜在肌肉活检的散在萎缩纤维中发现了异常线粒体。讨论了该综合征及其在儿科鉴别诊断中的相关性。