[
    {
        "id": "osp-11482",
        "type": "article-journal",
        "title": "Oculocutaneous Albinism associated with Axenfeld’s Anomaly: Three case reports",
        "author": [
            {
                "family": "Keshav",
                "given": "B R."
            },
            {
                "family": "Mohammed",
                "given": "Mahmood J."
            },
            {
                "family": "Nasir",
                "given": ""
            }
        ],
        "URL": "https://omanscience.com/ar/articles/oculocutaneous-albinism-associated-with-axenfeld-s-anomaly-three-case-reports",
        "language": "en",
        "issued": {
            "date-parts": [
                [
                    2025
                ]
            ]
        },
        "container-title": "Sultan Qaboos University Medical Journal",
        "volume": "10",
        "issue": "1",
        "page": "111-113",
        "DOI": "10.18295/2075-0528.1168",
        "publisher": "Sultan Qaboos University",
        "ISSN": "2075-051X",
        "abstract": "Oculocutaneous albinism and anterior mesodermal dysgenesis are well-known heritable conditions, but their occurrence in association has only been rarely reported. We present cases of three siblings of a family with identical presentation suggesting that this association may be more than just a coincidence. This association is worth noting, as this could be one of the causes of ocular morbidity and poor vision in oculocutaneous albinism."
    }
]