الملخص
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.
الكلمات المفتاحية
بيانات النشر
- المعرّف الرقمي
- 10.4103/0974-620x.99377
- المجلة
- المجلة العُمانية لطب العيون, 5(2), 115-117
- الناشر
- منشورات ميدنو
- وصول مفتوح
- وصول مفتوح ذهبي
اقتبس هذه المقالة
APA 7
Ahmad, S. S., & Ghani, S. A. (2012). Kearns-Sayre syndrome: An unusual ophthalmic presentation. Oman Journal of Ophthalmology, 5(2), 115-117. https://doi.org/10.4103/0974-620x.99377
MLA 9
Ahmad, Syed S, and Shuaibah A Ghani. "Kearns-Sayre syndrome: An unusual ophthalmic presentation." Oman Journal of Ophthalmology, vol. 5, no. 2, 2012, pp. 115-117. https://doi.org/10.4103/0974-620x.99377.
شيكاغو (المؤلف–التاريخ)
Ahmad, Syed S, and Shuaibah A Ghani. 2012. "Kearns-Sayre syndrome: An unusual ophthalmic presentation." Oman Journal of Ophthalmology 5 (2): 115-117. https://doi.org/10.4103/0974-620x.99377.
هارفارد
Ahmad, S. S. and Ghani, S. A. (2012) 'Kearns-Sayre syndrome: An unusual ophthalmic presentation', Oman Journal of Ophthalmology, 5(2), pp. 115-117. doi:10.4103/0974-620x.99377.
فانكوفر
Ahmad SS, Ghani SA. Kearns-Sayre syndrome: An unusual ophthalmic presentation. Oman Journal of Ophthalmology. 2012;5(2):115-117. doi:10.4103/0974-620x.99377
IEEE
S. S. Ahmad, and S. A. Ghani, "Kearns-Sayre syndrome: An unusual ophthalmic presentation," Oman Journal of Ophthalmology, vol. 5, no. 2, pp. 115-117, 2012, doi: 10.4103/0974-620x.99377.