Vock K, Todt H, Fötzsch R, Fischer R
Abteilung für Neuropädiatrie, Medizinischen Akademie Carl Gustav Carus, Dresden.
Kinderarztl Prax. 1990 Feb;58(2):93-7.
Progressive external ophthalmoplegia has generally been considered a brainstem syndrome, but new investigative techniques have identified a variety of etiologies. We report a 17-year-old girl in whom Kearns-Sayre syndrome presented as unilateral ptosis with progression to bilateral ptosis, and discuss the clinical, biochemical, electrophysiological, histopathological and computerized tomographical findings.
进行性眼外肌麻痹通常被认为是一种脑干综合征，但新的研究技术已发现了多种病因。我们报告了一名17岁女孩，其患有凯-赛综合征，最初表现为单侧上睑下垂，随后发展为双侧上睑下垂，并讨论了临床、生化、电生理、组织病理学和计算机断层扫描结果。
