Ts. Chang et al., CORNEAL DECOMPENSATION IN MITOCHONDRIAL OPHTHALMOPLEGIA PLUS (KEARNS-SAYRE) SYNDROME - A CLINICOPATHOLOGICAL CASE-REPORT, Cornea, 13(3), 1994, pp. 269-273
The authors describe the clinical, molecular genetic, and pathologic f
indings of a patient with corneal decompensation associated with the m
itochondrial ophthalmoplegia plus (Kearns-Sayre) syndrome. Ultrastruct
urally abnormal mitochondria were observed and possibly implicate this
organelle in the pathogenesis of corneal edema.