Chang T S, Johns D R, Stark W J, Drachman D B, Green W R
Eye Pathology Laboratory, Wilmer Ophthalmologic Institute, Johns Hopkins Medical Institutions, Baltimore, Maryland.
Cornea. 1994 May;13(3):269-73. doi: 10.1097/00003226-199405000-00014.
The authors describe the clinical, molecular genetic, and pathologic findings of a patient with corneal decompensation associated with the mitochondrial ophthalmoplegia plus (Kearns-Sayre) syndrome. Ultrastructurally abnormal mitochondria were observed and possibly implicate this organelle in the pathogenesis of corneal edema.
作者描述了一名患有与线粒体性眼肌麻痹加综合征（凯-塞尔综合征）相关的角膜失代偿患者的临床、分子遗传学和病理学发现。超微结构观察到线粒体异常，这可能与此细胞器在角膜水肿发病机制中起作用有关。
