[
    {
        "id": "osp-11997",
        "type": "article-journal",
        "title": "Branch retinal artery occlusion in a young patient with Mayer-Rokitansky-Küster-Hauser type 2 syndrome",
        "author": [
            {
                "family": "Bedwal",
                "given": "Anita"
            },
            {
                "family": "Banerjee",
                "given": "Mousumi"
            },
            {
                "family": "Rewri",
                "given": "Parveen"
            }
        ],
        "URL": "https://omanscience.com/ar/articles/branch-retinal-artery-occlusion-in-a-young-patient-with-mayer-rokitansky-k-ster-hauser-type-2-syndrome",
        "language": "en",
        "issued": {
            "date-parts": [
                [
                    2024
                ]
            ]
        },
        "container-title": "Oman Journal of Ophthalmology",
        "volume": "17",
        "issue": "3",
        "page": "393-395",
        "DOI": "10.4103/ojo.ojo_48_24",
        "publisher": "Medknow Publications",
        "ISSN": "0974-620X",
        "abstract": "Retinal vascular occlusions are rare in young people, and any occlusion warrants an extensive clinical evaluation to establish the etiology. Cardiac malformations are a source of embolism. We present a case of atrial septal defect (ASD) in a patient with type II Mayer-Rokitansky-Küster-Hauser syndrome, leading to unilateral branch retinal arterial occlusion (BRAO) in a young woman. A 21-year-old woman presented with sudden, painless, blurring of vision, and a superior visual field defect in her right eye. A fundus examination confirmed the BRAO diagnosis. Ocular and systemic evaluation revealed primary amenorrhea, ASD, ectopic kidneys, and pelvic cyst. Any vascular occlusion in a young patient must be thoroughly evaluated, including a detailed systemic history."
    }
]