[
    {
        "id": "osp-12919",
        "type": "article-journal",
        "title": "Kearns-Sayre syndrome: An unusual ophthalmic presentation",
        "author": [
            {
                "family": "Ahmad",
                "given": "Syed S"
            },
            {
                "family": "Ghani",
                "given": "Shuaibah A"
            }
        ],
        "URL": "https://omanscience.com/en/articles/kearns-sayre-syndrome-an-unusual-ophthalmic-presentation",
        "language": "en",
        "issued": {
            "date-parts": [
                [
                    2012
                ]
            ]
        },
        "container-title": "Oman Journal of Ophthalmology",
        "volume": "5",
        "issue": "2",
        "page": "115-117",
        "DOI": "10.4103/0974-620x.99377",
        "publisher": "Medknow Publications",
        "ISSN": "0974-620X",
        "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."
    }
]