[
    {
        "id": "osp-11838",
        "type": "article-journal",
        "title": "A unique case report of Wildervanck syndrome in association with facial nerve paresis and arachnodactyly",
        "author": [
            {
                "family": "Surekha",
                "given": "P"
            },
            {
                "family": "Kavitha",
                "given": "V"
            },
            {
                "family": "Penugonda",
                "given": "Pravallika"
            },
            {
                "family": "Heralgi",
                "given": "Mallikarjun M"
            }
        ],
        "URL": "https://omanscience.com/ar/articles/a-unique-case-report-of-wildervanck-syndrome-in-association-with-facial-nerve-paresis-and-arachnodactyly",
        "language": "en",
        "issued": {
            "date-parts": [
                [
                    2026
                ]
            ]
        },
        "container-title": "Oman Journal of Ophthalmology",
        "volume": "19",
        "issue": "2",
        "page": "259-262",
        "DOI": "10.4103/ojo.ojo_130_25",
        "publisher": "Medknow Publications",
        "ISSN": "0974-620X",
        "abstract": "Wildervanck syndrome, also called as cervico-oculo-acoustic syndrome. This is characterized by the triad of Klippel-Feil syndrome, Duane retraction syndrome, and congenital deafness. Other associations described are cardiovascular and musculoskeletal abnormalities. Some reports, in fact, state that nearly one percent of hearing-impaired females may be affected by Wildervanck syndrome. In our case report, a child who had the complete triad of the syndrome along with arachnodactyly (long slender digits), camptodactyly, short stature, and facial nerve paresis has been described."
    }
]