1.
Oman Journal of Ophthalmology. 2012; 5 (2): 115-117
in English
| IMEMR
| ID: emr-133700
ABSTRACT
Kearns-Sayre syndrome [KSS] belongs to the group of neuromuscular disorders known as mitochondrial encephalomyopathies. It has characteristic syndromal features, which include: chronic progressive external ophthalmoplegia, bilateral atypical pigmentary retinopathy, and cardiac conduction abnormalities. So far, only a single case has been reported where a patient with KSS had a normal retina. Herein, we report this extremely rare variant of KSS, which not only presented later than the normal age of presentation, but also had minimal pigmentary retinopathy
2.
Medical Spectrum [The]. 1993; 14 (19-20): 22-3
in English
| IMEMR
| ID: emr-29410