[
    {
        "id": "osp-12364",
        "type": "article-journal",
        "title": "Spontaneously resolved severe retinopathy associated with aplastic anemia",
        "author": [
            {
                "family": "Mal",
                "given": "Washoo"
            },
            {
                "family": "Al-Abri",
                "given": "Mohamed"
            }
        ],
        "URL": "https://omanscience.com/en/articles/spontaneously-resolved-severe-retinopathy-associated-with-aplastic-anemia",
        "language": "en",
        "issued": {
            "date-parts": [
                [
                    2021
                ]
            ]
        },
        "container-title": "Oman Journal of Ophthalmology",
        "volume": "14",
        "issue": "2",
        "page": "117-119",
        "DOI": "10.4103/ojo.ojo_117_21",
        "publisher": "Medknow Publications",
        "ISSN": "0974-620X",
        "abstract": "Aplastic anemia is a rare, usually autoimmune disorder of bone marrow stem cells leading to pancytopenia and hypoplastic marrow that presents with anemia, infection or bleeding which can be potentially sight and life-threatening. Patients with aplastic anemia may present with various ocular manifestations; lid and orbital hematoma, sub-conjunctival hemorrhage, sudden visual loss due to vitreous hemorrhage or retinopathy and optic disc edema. A young male patient had symptomatic sever bilateral hemorrhagic retinopathy secondary to aplastic anemia; succeeding systemic allogenic hematopoietic stem-cell transplantation showed almost complete spontaneous resolution of the retinopathy and significant improvement in vision over a period of 16 weeks."
    }
]